AU2013348009C1 - Substituted reverse pyrimidine Bmi-1 inhibitors - Google Patents

Substituted reverse pyrimidine Bmi-1 inhibitors Download PDF

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AU2013348009C1
AU2013348009C1 AU2013348009A AU2013348009A AU2013348009C1 AU 2013348009 C1 AU2013348009 C1 AU 2013348009C1 AU 2013348009 A AU2013348009 A AU 2013348009A AU 2013348009 A AU2013348009 A AU 2013348009A AU 2013348009 C1 AU2013348009 C1 AU 2013348009C1
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pyrimidine
benzimidazol
fluoro
diamine
phenyl
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Ramil BAIAZITOV
Liangxian Cao
Thomas W. Davis
Wu Du
Chang-Sun Lee
Ronggang Liu
Young-Choon Moon
Steven D. Paget
Hongyu Ren
Nadiya Sydorenko
Richard Gerald Wilde
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PTC Therapeutics Inc
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    • C—CHEMISTRY; METALLURGY
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
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    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
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    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

Amine substituted reverse pyrimidine compounds and forms thereof that inhibit the function and reduce the level of B-cell specific Moloney murine leukemia virus integration site 1 (Bmi-1) protein and methods for their use to inhibit Bmi-1 function and reduce the level of Bmi-1 to treat a cancer mediated by Bmi-1 are described herein.

Description

Substituted Reverse Pyrimidine Bmi-1 Inhibitors INTRODUCTION
Substituted reverse pyrimidine compounds that inhibit the function of the B-cell specific Moloney murine leukemia virus integration site 1 (Bmi-1) protein and reduce the level thereof and methods of using such compounds to treat a cancer mediated by Bmi-1 are described. More particularly, amine substituted reverse pyrimidine compounds that inhibit Bmi-1 function and reduce the level of Bmi-1 are useful for treating a cancer mediated by Bmi-1.
BACKGROUND
Bmi-1 was originally identified by its over-expression in various leukemias and lymphomas. Subsequently, Bmi-1 has been shown to have oncogenic activity when overexpressed in normal cells and to play a role in the maintenance of cancer stem cell populations. Bmi-1 is elevated in many tumor types and is important in hematologic cancers and many solid tumors, including brain cancers. Reduction of Bmi-1 levels in tumor cells by siRNA causes apoptosis and/or cell senescence and increases susceptibility to cytotoxic agents. Bmi-1 serves as the key regulatory component of the PRC1 complex (polycomb repressive complex-1), but has no enzymatic activity. Therefore, targeting Bmi-1 by traditional drug discovery methods has been problematic.
Since Bmi-1 levels within cells are tightly regulated through both transcriptional and post-transcriptional mechanisms, this regulation can be exploited to target this important protein. Accordingly, there remains a need to provide compounds that inhibit Bmi-1 function and reduce the level of Bmi-1 to treat a cancer mediated by Bmi-1.
SUMMARY
Certain amine substituted reverse pyrimidine compounds that inhibit Bmi-1 function and reduce the level of Bmi-1 and methods for their use to treat a cancer mediated by Bmi-1 are described herein.
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PCT/US2013/071132
A compound of Formula (I) is described:
Figure AU2013348009C1_D0001
wherein X, Ri, R2, R3 and R4 are as defined herein, including forms and pharmaceutical compositions thereof, and methods of using such compounds, forms or compositions thereof to treat a cancer mediated by Bmi-1 in a human subject in need thereof.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 demonstrates the dose dependent reduction of a CSC population in a BXD GBM model as the result of treatment with a compound of Formula (I), or a form thereof.
Figure 2 demonstrates the reduction of a CSC population in a BXD GBM model as the result of treatment with a compound of Formula (I), or a form thereof.
Figure 3 demonstrates the reduction of monolayer and neurosphere CSC populations in a tumorosphere assay as the result of contacting the cells with a compound of Formula (I), or a form thereof.
Figure 4 demonstrates the comparative effect on survival of mice treated with vehicle, temozolomide or a compound of Formula (I), or a form thereof, in an orthotopic model of glioblastoma.
DETAILED DESCRIPTION
Amine substituted reverse pyrimidine compounds for use in inhibiting Bmi-1 function and reducing the level of Bmi-1 and in methods for treating a cancer mediated by Bmi-1 are described.
In one embodiment is a compound of Formula (I):
Figure AU2013348009C1_D0002
WO 2014/081906
PCT/US2013/07U32 or a form thereof, wherein
Ri is heteroaryl or heterocyclyl optionally substituted on a carbon atom ring member with one, two, three or four R5 substituents, or on a nitrogen atom ring member with an oxygen atom substituent to form an N-oxide;
X is N or N substituted with an oxygen atom substituent to form an N-oxide;
R2 is hydrogen, cyano, halo, hydroxyl, nitro, Ci.galkyl, hydroxyl-Ci.galkyl, Ci.galkoxy, amino, Ci-galkyl-amino, (Ci„8alkyl)2-amino, hydroxyl-amino, hydroxyl-Ci-galkyl-amino, Ci-salkoxy-Ci^alkyl-amino, Ci_salkyl-thio, Ci-galkyl-carbonyl, Ci.galkyl-carbonyl-amino, amino-carbonyl, Ci-galkyl-amino-carbonyl, (Ci.galkyl^-amino-carbonyl, amino-carbonyl-amino, Ci_8alkyl-arnino-carbonyl-amino, (Ci.8alkyl)2-amino-carbonyl-amino, Ci-8alkoxy-carbonyl, Ci-salkoxy-carbonyl-amino, amino-sulfonyl, Ci_8alkyl-amino-sulfonyl, (Ci_8alkyl)2-amino-sulfonyl, amino-sulfonyl-amino, Ci-8alkyl-amino-sulfonyl-amino, (Ci_8alkyl)2-amino-sulfonyl-amino, P(O)(R7)2-amino or heteroaryl, wherein heteroaryl is optionally substituted with one, two, three or four Ci-salkyl substituents;
R3 is hydrogen, cyano, halo, Ci-galkyl, amino, Ci-salkyl-amino or (Ci_8alkyl)2-amino;
R4 is C3-i4cycloalkyl, aryl, heteroaryl or heterocyclyl, each optionally substituted with one, two, three or four R6 substituents;
R5 is independently selected from cyano, halo, hydroxyl, nitro, oxo, Ci^alkyl, cyano-Ci-salkyl, halo-Chalky], hydroxyl-Ci-salkyl, Ci_8alkoxy, Cj-salkoxy-Ci-salkyl, halo-Ci-salkoxy, C2-8alkenyl, Ci_8alkoxy-C2-8alkenyl, C2-8alkynyl, Ci-8alkoxy-C2-8alkynyl, carboxyl, amino, Ci^alkyl-amino, (Ci_8alkyl)2-amino, amino-Ci-salkyl, Ci-salkyl-amino-Ci-salkyl, (Ci-salkyl^-amino-Ci-salkyl, hydroxyl-Ci-salkyl-amino, hydroxyl-Ci-salkyl-amino-Ci-salkyl, hydroxyl-Ci -salkyl-amino-C 1 ^alkyl-amino, Cj-salkyl-thio, Cj-salkyl-carbonyl, Ci-salkyl-carbonyl-amino, Cj-salkyl-carbonyl-oxy, Cj^alkyl-carbonyl-oxy-Ci-salkyl, Ci_8alkoxy-carbonyl, Ci^alkoxy-carbonyl-Ci^alkyl, Ci^alkoxy-carbonyl-amino, Ci.galkyl-sulfonyl, CYncycloalkyl, aryl, aryl-Ci^alkyl, aryl-amino, aryl-Ci_8alky-amino, heteroaryl, heteroaryl-Ci.8alkyl or heterocyclyl, wherein C3.i4cycloalkyl, aryl, heteroaryl or heterocyclyl and the aryl and heteroaryl portions of aryl-Ci-8alkyl, aryl-amino, aryl-Ci-galky-amino and heteroaryl-Ci_8alkyl are each
WO 2014/081906
PCT/US2013/071132 optionally substituted with one, two, three or four halo, Ci_8alkyl, halo-Ci_8alkyl, hydroxyl-Cugalkyl, Cpgalkoxy, halo-Ci^alkoxy, hydroxyl-Ci^alkoxy or carboxyl substituents;
Rf, is independently selected from cyano, halo, hydroxyl, nitro, Ci-8alkyl, halo-Ci_8alkyl, hydroxyl-Ci_8alkyl, Cm alkoxy, halo-Ci.g alkoxy, C2-8alkenyl, Ci_8alkoxy-C2-8alkenyl, C2-8alkynyl, Ci-8alkoxy-C2-8alkynyl, carboxyl, formyl, formyl-oxy, Ci-salkyl-carbonyl, halo-Ci.galkyl-carbonyl, Ci_8alkyl-thio, halo-Ci^alkyl-thio, amino, Ci.galkyl-amino, (C].8alkyl)2-amino, Ci_8alkyl-carbonyl, Ci.8alkyl-carbonyl-oxy, Ci.8alkyl-carbonyl-oxy-Ci_8alkyl, Ci_8alkoxy-carbonyl, halo-Ci_8alkoxy-carbonyl, Ci-galkoxy-carbonyl-Ci-salkyl, Ci_8alkoxy-carbonyl-amino, Ci.8alkoxy-carbonyl-amino-Ci_8alkyl, amino-carbonyl, Ci-8alkyl-amino-carbonyl, (C i _8alkyl)2-amino-carbonyl, C i _8alkyl-carbonyl-amino, Ci.8alkyl-carbonyl-amino-Ci-8alkyl, amino-Ci-salkyl, Ci_8alkyl-amino-Ci-8alkyl, (Ci.8alkyl)2-amino-Ci_8alkyl, amino-Ci_8alkyl-amino, Ci-8alkyl-amino-Ci.8alkyl-amino, (Ci_8alkyl)2-amino-Ci.8alkyl-amino, hydroxyl-Ci_8alkyl-amino, hydroxyl-Ci-8alkyl-amino-Ci.8alkyl, hydroxyl-Ci_8alkyl-amino-Ci-8alkyl-amino, imino-Ci_8alkyl, hydroxyl-imino-C i .8alkyl, C i _8alkoxy-imino-C i _8alkyl, C i _8 alkyl-sulfonyl, halo-Ci_8alkyl-sulfonyl, amino-sulfonyl, Ci_8alkyl-amino-sulfonyl, (Ci_8alkyl)2-amino-sulfonyl, B(OR8)2, C3_i4cycloalkyl, heterocyclyl, aryl or heteroaryl, wherein C3_i4cycloalkyl, heterocyclyl, aryl, and heteroaryl are each optionally substituted with one, two, three or four halo or Ci_8alkyl substituents;
R7 is independently hydroxyl or (Ci_8alkoxy)n, wherein n represents an integer from 1 to 5; and,
R8 is independently hydrogen or Ci_8alkyl.
Another embodiment includes a compound of Formula (I), wherein R| is optionally substituted heteroaryl or heterocyclyl selected from ΙΗ-pyrazolyl, lH-imidazolyl, 1,2oxazolyl, pyridinyl, ΙΗ-indolyl, 2H-indazolyl, 4,5,6,7-tetrahydro-2H-indazolyl, 1Hbenzimidazolyl, imidazo[2,l-b][l,3]thiazolyl, pyrazolo[l,5-a]pyridinyl, pyrazolo[l,5c]pyrimidinyl, imidazo[l,2-a]pyridinyl, 5,6,7,8-tetrahydroimidazo[l,2-a]pyridinyl, 1H4
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PCT/US2013/071132 imidazo[4,5-b]pyridinyl, lH-imidazo[4,5-c]pyridinyl, 4,5,6,7-tetrahydro-3H-imidazo[4,5c]pyridinyl, imidazo[l,2-a]pyrazinyl, imidazo[l,2-a]pyrimidinyl, 7H-purinyl or quinolinyl.
Another embodiment includes a compound of Formula (I), wherein Rj is optionally substituted heteroaryl or heterocyclyl selected from ΙΗ-pyrazolyl, ΙΗ-imidazolyl, 1,2oxazolyl, pyridinyl, ΙΗ-indolyl, 2H-indazolyl, 4,5,6,7-tetrahydro-2H-indazolyl, 1Hbenzimidazolyl, imidazo[2,1 -b] [ 1,3]thiazolyl, pyrazolo[ 1,5-a]pyridinyl, imidazo[ 1,2-a]pyridinyl, 5,6,7,8-tetrahydroimidazof 1,2-a]pyridinyl, 1 H-imidazof4,5b]pyridinyl, lH-imidazo[4,5-c]pyridinyl, 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridinyl, imidazo[l,2-a]pyrazinyl, imidazo[l,2-a]pyrimidinyl, 7H-purinyl or quinolinyl.
Another embodiment includes a compound of Formula (I), wherein Ri is optionally substituted heteroaryl or heterocyclyl selected from lH-pyrazol-4-yl, lH-imidazol-l-yl, lH-imidazol-5-yl, 1,2-oxazol-4-yl, l,2-oxazol-5-yl, pyridin-4-yl, ΙΗ-indol-l-yl, lH-indol-3yl, lH-indol-4-yl, 2H-indazol-3-yl, 4,5,6,7-tetrahydro-2H-indazol-3-yl, lH-benzimidazol-1yl, imidazo[2,l-b][l,3]thiazol-5-yl, pyrazolofl,5-a]pyridin-2-yl, pyrazolo[l,5-a]pyridin-3-yl, pyrazolof1,5-a]pyridin-7-yl, pyrazolo[ 1,5-c]pyrimidin-3-yl, imidazof 1,2-a]pyridin-2-yl, imidazof 1,2-a]pyridin-3-yl, imidazof 1,2-a]pyridin-5-yl, 5,6,7,8-tetrahydroimidazof 1,2a]pyridin-3-yl, lH-imidazo[4,5-b]pyridin-l-yl, lH-imidazo[4,5-c]pyridin-l-yl, 4,5,6,7tetrahydro-3H-imidazo[4,5-c]pyridin-3-yl, imidazof l,2-a]pyrazin-3-yl, imidazof 1,2a]pyrimidin-3-yl, 7H-purin-7-yl or quinolin-4-yl.
Another embodiment includes a compound of Formula (I), wherein Rj is optionally substituted heteroaryl or heterocyclyl selected from lH-pyrazol-4-yl, lH-imidazol-l-yl, lH-imidazol-5-yl, l,2-oxazol-4-yl, l,2-oxazol-5-yl, pyridin-4-yl, lH-indol-l-yl, lH-indol-4-yl, 2H-indazol-3-yl, 4,5,6,7-tetrahydro-2H-indazol-3-yl, lH-benzimidazol-l-yl, imidazo[2,l-b][l,3]thiazol-5-yl, pyrazolo[l,5-a]pyridin-3-yl, pyrazolo[l,5-a]pyridin-7-yl, imidazof 1,2-a]pyridin-3-yl, imidazof 1,2-a]pyridin-5-yl, 5,6,7,8-tetrahydroimidazof 1,2a]pyridin-3-yl, lH-imidazo[4,5-b]pyridin-l-yl, lH-imidazof4,5-c]pyridin-l-yl, 4,5,6,7tetrahydro-3H-imidazo[4,5-c]pyridin-3-yl, imidazofl,2-a]pyrazin-3-yl, imidazofl,2-a]pyrimidin-3-yl, 7H-purin-7-yl or quinolin-4-yl.
Another embodiment includes a compound of Formula (I), wherein R| is optionally substituted heteroaryl or heterocyclyl selected from lH-pyrazol-4-yl, lH-imidazol-l-yl, lH-imidazol-5-yl, 1,2-oxazol-4-yl, l,2-oxazol-5-yl, pyridin-4-yl, lH-indol-l-yl,
WO 2014/081906
PCT/US2013/07U32 lH-indol-4-yl, 2H-indazol-3-yl, 4,5,6,7-tetrahydro-2H-indazol-3-yl, lH-benzimidazol-l-yl, imidazo[2,l-b][l,3]thiazol-5-yl, pyrazolof l,5-a]pyridin-3-yl, pyrazolo[l,5-a]pyridin-7-yl, imidazo[l,2-a]pyridin-3-yl, imidazof l,2-a]pyridin-5-yl, 5,6,7,8-tetrahydroimidazo[l,2a]pyridin-3-yl, lH-imidazo[4,5-b]pyridin-l-yl, lH-imidazo[4,5-c]pyridin-l-yl, 4,5,6,7tetrahydro-3H-imidazo[4,5-c]pyridin-3-yl, 7H-purin-7-yl or quinolin-4-yl.
Another embodiment includes a compound of Formula (I), wherein Rj is optionally substituted heteroaryl selected from lH-pyrazolyl, lH-imidazolyl, 1,2-oxazolyl, pyridinyl, ΙΗ-indolyl, 2H-indazolyl, lH-benzimidazolyl, imidazo[2,l-b][l,3]thiazolyl, pyrazolo[ 1,5-a]pyridinyl, pyrazolof 1,5-c]pyrimidinyl, imidazo[ 1,2-a]pyridinyl, lH-imidazo[4,5-b]pyridinyl, lH-imidazo[4,5-c]pyridinyl, imidazof 1,2-a]pyrazinyl, imidazo[l,2-a]pyrimidinyl, 7H-purinyl or quinolinyl.
Another embodiment includes a compound of Formula (I), wherein Ri is optionally substituted heteroaryl selected from lH-pyrazolyl, ΙΗ-imidazolyl, 1,2-oxazolyl, pyridinyl, ΙΗ-indolyl, 2H-indazolyl, ΙΗ-benzimidazolyl, imidazo[2,l-b][l,3]thiazolyl, pyrazolo[l,5-a]pyridinyl, imidazofl,2-a]pyridinyl, lH-imidazo[4,5-b]pyridinyl, 1Himidazo[4,5-c]pyridinyl, imidazofl,2-a]pyrazinyl, imidazofl,2-a]pyrimidinyl, 7H-purinyl or quinolinyl.
Another embodiment includes a compound of Formula (I), wherein Ri is optionally substituted heteroaryl selected from lH-pyrazolyl, ΙΗ-imidazolyl, 1,2-oxazolyl, pyridinyl, ΙΗ-indolyl, 2H-indazolyl, ΙΗ-benzimidazolyl, imidazo[2,l-b][l,3]thiazolyl, pyrazolo[l,5-a]pyridinyl, imidazofl,2-a]pyridinyl, lH-imidazof4,5-b]pyridinyl, 1Himidazo[4,5-c]pyridinyl, 7H-purinyl or quinolinyl.
Another embodiment includes a compound of Formula (I), wherein R | is optionally substituted heteroaryl selected from lH-pyrazolyl, ΙΗ-indolyl, lH-benzimidazolyl, pyrazolof 1,5-a]pyridinyl, imidazof 1,2-a]pyridinyl, lH-imidazo[4,5-b]pyridinyl, imidazofl,2-a]pyrazinyl or imidazof 1,2-a]pyrimidinyl.
Another embodiment includes a compound of Formula (I), wherein R| is optionally substituted heteroaryl selected from lH-pyrazolyl, ΙΗ-indolyl, lH-benzimidazolyl, pyrazolofl,5-a]pyridinyl, imidazof 1,2-a]pyridinyl or lH-imidazo[4,5-b]pyridinyl.
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PCT/US2013/071132
Another embodiment includes a compound of Formula (I), wherein Rj is optionally substituted heteroaryl selected from imidazo[l,2-a]pyrazinyl or imidazo[l,2-a]pyrimidinyl.
Another embodiment includes a compound of Formula (I), wherein Rj is optionally substituted imidazof 1,2-a]pyrazinyl.
Another embodiment includes a compound of Formula (I), wherein Rj is optionally substituted imidazof 1,2-a]pyrimidinyl.
Another embodiment includes a compound of Formula (I), wherein Rj is optionally substituted heteroaryl selected from lH-pyrazol-4-yl, lH-imidazol-l-yl, lH-imidazol-5-yl, l,2-oxazol-4-yl, l,2-oxazol-5-yl, pyridin-4-yl, lH-indol-l-yl, lH-indol-3-yl, lH-indol-4-yl, 2H-indazol-3-yl, 1 H-benzimidazol-1 -yl, imidazo[2,1 -b] [ 1,3]thiazol-5-yl, pyrazolo[l,5-a]pyridin-2-yl, pyrazolo[l,5-a]pyridin-3-yl, pyrazolo[l,5-a]pyridin-7-yl, pyrazolof 1,5-c]pyrimidin-3-yl, imidazof 1,2-a]pyridin-2-yl, imidazof 1,2-a]pyridin-3-yl, imidazofl,2-a]pyridin-5-yl, lH-imidazof4,5-b]pyridin-l-yl, lH-imidazo[4,5-c]pyridin-l-yl, imidazofl,2-a]pyrazin-3-yl, imidazo[l,2-a]pyrimidin-3-yl, 7H-purin-7-yl or quinolin-4-yl.
Another embodiment includes a compound of Formula (I), wherein R] is optionally substituted heteroaryl selected from lH-pyrazol-4-yl, lH-imidazol-l-yl, lH-imidazol-5-yl,
1.2- oxazol-4-yl, l,2-oxazol-5-yl, pyridin-4-yl, lH-indol-l-yl, lH-indol-4-yl, 2H-indazol-3-yl, lH-benzimidazol-l-yl, imidazof2,l-b][l,3]thiazol-5-yl, pyrazolofl,5-a]pyridin-3-yl, pyrazolofl,5-a]pyridin-7-yl, imidazo[l,2-a]pyridin-3-yl, imidazo[l,2-a]pyridin-5-yl, lH-imidazo[4,5-b]pyridin-l-yl, lH-imidazof4,5-c]pyridin-l-yl, imidazo[l,2-a]pyrazin-3-yl, imidazof l,2-a]pyrimidin-3-yl, 7H-purin-7-yl or quinolin-4-yl.
Another embodiment includes a compound of Formula (I), wherein Ri is optionally substituted heteroaryl selected from lH-pyrazol-4-yl, lH-imidazol-l-yl, lH-imidazol-5-yl,
1.2- oxazol-4-yl, l,2-oxazol-5-yl, pyridin-4-yl, lH-indol-l-yl, lH-indol-4-yl, 2H-indazol-3-yl, ΙΗ-benzimidazol-l-yl, imidazo[2,l-b][l,3]thiazol-5-yl, pyrazolofl,5-a]pyridin-7-yl, imidazofl,2-a]pyridin-5-yl, lH-imidazof4,5-b]pyridin-l-yl, lH-imidazo[4,5-c]pyridin-l-yl, imidazofl,2-a]pyrazin-3-yl, imidazofl,2-a]pyrimidin-3-yl, 7H-purin-7-yl or quinolin-4-yl.
Another embodiment includes a compound of Formula (I), wherein R| is optionally substituted heteroaryl selected from lH-pyrazol-4-yl, lH-indol-l-yl, lH-indol-3-yl, lH-indol-4-yl, ΙΗ-benzimidazol-l-yl, pyrazolof 1,5-a]pyridin-2-yl, pyrazolofl,5-a]pyridin-37
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PCT/US2013/071132 yl, pyrazolo[l,5-a]pyridin-7-yl, imidazo[l,2-a]pyridin-2-yl, imidazo[l,2-a]pyridin-3-yl, imidazo[l,2-a]pyridin-5-yl, lH-imidazo[4,5-b]pyridin-l-yl, imidazo[l,2-a]pyrazin-3-yl or imidazo[l ,2-a]pyrimidin-3-yl.
Another embodiment includes a compound of Formula (I), wherein Ri is optionally substituted heteroaryl selected from lH-pyrazol-4-yl, lH-indol-3-yl, lH-benzimidazol-l-yl, pyrazolo[l,5-a]pyridin-2-yl, pyrazolo[l,5-a]pyridin-3-yl, imidazo[l,2-a]pyridin-2-yl, imidazo[l,2-a]pyridin-3-yl, lH-imidazo[4,5-b]pyridin-l-yl, imidazo[l,2-a]pyrazin-3-yl or imidazo [ 1,2-a]pyrimidin-3 -yl.
Another embodiment includes a compound of Formula (I), wherein Ri is optionally substituted heteroaryl selected from lH-pyrazol-4-yl, lH-indol-3-yl, lH-benzimidazol-l-yl, pyrazolo[l,5-a]pyridin-3-yl, imidazo[l,2-a]pyridin-3-yl, lH-imidazo[4,5-b]pyridin-l-yl, imidazo[l,2-a]pyrazin-3-yl or imidazo[l,2-a]pyrimidin-3-yl.
Another embodiment includes a compound of Formula (I), wherein Ri is optionally substituted imidazo[l,2-a]pyrazin-3-yl.
Another embodiment includes a compound of Formula (I), wherein Rj is optionally substituted imidazof 1,2-a]pyrimidin-3-yl.
Another embodiment includes a compound of Formula (I), wherein Rj is optionally substituted heterocyclyl selected from 4,5,6,7-tetrahydro-2H-indazolyl, 5,6,7,8tetrahydroimidazo[l ,2-a]pyridinyl or 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridinyl.
Another embodiment includes a compound of Formula (I), wherein Ri is optionally substituted heterocyclyl selected from 4,5,6,7-tetrahydro-2H-indazol-3-yl, 5,6,7,8tetrahydroimidazo[l ,2-a]pyridin-3-yl or 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridin-3-yl.
Another embodiment includes a compound of Formula (I), wherein X is N.
Another embodiment includes a compound of Formula (I), wherein X is N substituted with an oxygen atom substituent to form an N-oxide.
Another embodiment includes a compound of Formula (I), wherein R2 is cyano, halo, hydroxyl, nitro, Cj-galkyl, hydroxyl-Ci^alkyl, C|^alkoxy, amino, Ci^alkyl-amino, (Ci_8alkyl)2-amino, hydroxyl-amino, hydroxyl-Ci.galkyl-amino, Ci-salkoxy-Ci-salkyl-amino, Cj.salkyl-thio, Chalky!-carbonyl, Cj.salkyl-carbonyl-amino, amino-carbonyl,
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Ci-salkyl-amino-carbonyl, (Cj.8alkyl)2-amino-carbonyl, amino-carbonyl-amino,
C i _8alkyl-amino-carbonyl-amino, (C i _8alkyl)2-amino-carbonyl-amino, C i .8alkoxy-carbonyl, Ci_8alkoxy-carbonyl-amino, amino-sulfonyl, Cb8alkyl-amino-sulfonyl, (Ci_8alkyl)2-amino-sulfonyl, amino-sulfonyl-amino, Ci_8alkyl-amino-sulfonyl-amino, (Ci_8alkyl)2-amino-sulfonyl-amino, P(O)(R7)2-amino or heteroaryl, wherein heteroaryl is optionally substituted with one, two, three or four Ci_8alkyl substituents.
Another embodiment includes a compound of Formula (I), wherein R2 is cyano, halo, nitro, Ci.8alkyl, hydroxyl-Ci_8alkyl, C].8alkoxy, amino, hydroxyl-amino, hydroxyl-Ci_8alkyl-amino, Ci.8alkoxy-Ci_8alkyl-amino, Ci_8alkyl-thio, amino-carbonyl, amino-carbonyl-amino, Ci_8alkoxy-carbonyl-amino, amino-sulfonyl-amino or heteroaryl, wherein heteroaryl is optionally substituted with one, two, three or four Ci_8alkyl substituents.
Another embodiment includes a compound of Formula (I), wherein R2 is cyano, halo, hydroxyl, nitro, C].8alkyl, hydroxyl-Ci_8alkyl, Ci_8alkoxy, amino, Ci_8alkyl-amino, (C].8alkyl)2-amino, hydroxyl-amino, hydroxyl-Ci_8alkyl-amino, Ci_8alkoxy-Ci_8alkyl-amino, Ci_8alkyl-thio, C].8alkyl-carbonyl, Ci^alkyl-carbonyl-amino, amino-carbonyl, Ci.8alkyl-amino-carbonyl, (Ci_8alkyl)2-amino-carbonyl, amino-carbonyl-amino, Ci_8alkyl-amino-carbonyl-amino, (Ci_8alkyl)2-amino-carbonyl-amino, Ci_8alkoxy-carbonyl, Ci_8alkoxy-carbonyl-amino, amino-sulfonyl, Ci_8alkyl-amino-sulfonyl, (Ci_8alkyl)2-amino-sulfonyl, amino-sulfonyl-amino, Ci_8alkyl-amino-sulfonyl-amino, (Ci-8alkyl)2-amino-sulfonyl-amino or P(O)(R7)2-amino.
Another embodiment includes a compound of Formula (I), wherein R2 is cyano, halo, nitro, Ci_8alkyl, hydroxyl-Ci_8alkyl, Ci_8alkoxy, amino, hydroxyl-amino, hydroxyl-Ci_8alkyl-amino, Ci-8alkoxy-Ci_8alkyl-amino, Ci_8alkyl-thio, amino-carbonyl, amino-carbonyl-amino, Ci_8alkoxy-carbonyl-amino or amino-sulfonyl-amino.
Another embodiment includes a compound of Formula (I), wherein R2 is heteroaryl, wherein heteroaryl is optionally substituted with one, two, three or four C].8alkyl substituents.
Another embodiment includes a compound of Formula (I), wherein R2 heteroaryl is optionally substituted lH-pyrrolyl.
Another embodiment includes a compound of Formula (I), wherein R2 heteroaryl is optionally substituted lH-pyrrol-l-yl.
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Another embodiment includes a compound of Formula (I), wherein R3 is hydrogen.
Another embodiment includes a compound of Formula (I), wherein R3 is cyano, halo, Ci-ealkyl, amino, Ci^alkyl-amino or (Ci.galkyl^-amino.
Another embodiment includes a compound of Formula (I), wherein R3 is cyano, halo, Ci_8alkyl or amino.
Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted C3_i4cycloalkyl selected from 2,3-dihydro-ΙΗ-indenyl; or, optionally substituted aryl selected from phenyl or naphthyl; or, optionally substituted heteroaryl selected from 1,3thiazolyl, 1,2-oxazolyl, pyridinyl, pyrimidinyl, ΙΗ-indolyl, benzofuranyl, benzooxazolyl, 1,3benzothiazolyl, quinolinyl or isoquinolinyl; or, optionally substituted heterocyclyl selected from 1,3-benzodioxolyl or 2,3-dihydro-l,4-benzodioxinyl.
Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted C3.i4cycloalkyl selected from 2,3-dihydro-lH-indenyl.
Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted C3_i4cycloalkyl selected from 2,3-dihydro-lH-inden-2-yl.
Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted aryl selected from phenyl or naphthyl.
Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted heteroaryl selected from 1,3-thiazolyl, 1,2-oxazolyl, pyridinyl, pyrimidinyl, 1Hindolyl, benzofuranyl, benzooxazolyl, 1,3-benzothiazolyl, quinolinyl or isoquinolinyl; or, optionally substituted heterocyclyl selected from 1,3-benzodioxolyl or 2,3-dihydro-1,4benzodioxinyl.
Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted heteroaryl selected from l,3-thiazol-2-yl, l,2-oxazol-5-yl, pyridin-2-yl, pyridin-3yl, pyrimidin-5-yl, lH-indol-5-yl, benzofuran-5-yl, benzooxazol-5-yl, l,3-benzothiazol-2-yl, quinolin-3-yl, quinolin-6-yl or isoquinolin-3-yl; or, optionally substituted heterocyclyl selected from l,3-benzodioxol-5-yl or 2,3-dihydro-l,4-benzodioxin-6-yl.
Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted heteroaryl selected from 1,3-thiazolyl, 1,2-oxazolyl, pyridinyl, pyridinyl,
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Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted heteroaryl selected from l,3-thiazol-2-yl, l,2-oxazol-5-yl, pyridin-2-yl, pyridin-3yl, pyrimidin-5-yl, lH-indol-5-yl, benzofuran-5-yl, benzooxazol-5-yl, l,3-benzothiazol-2-yl, quinolin-3-yl, quinolin-6-yl or isoquinolin-3-yl.
Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted heterocyclyl selected from 1,3-benzodioxolyl or 2,3-dihydro-l,4-benzodioxinyl.
Another embodiment includes a compound of Formula (I), wherein R4 is optionally substituted heterocyclyl selected from l,3-benzodioxol-5-yl or 2,3-dihydro-l,4-benzodioxin6-yl.
Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from cyano, halo, hydroxyl, nitro, Cj.salkyl, cyano-Cj^alkyl, halo-Ci.«alkyl, hydroxyl-C 1.3alkyl, C®alkoxy, Ci_8alkoxy-Ci-8alkyl, halo-Ci-salkoxy, C2-8alkenyl, Ci.8alkoxy-C2-salkenyl, carboxyl, amino, Chalky!-amino, Ci-8alkyl-amino-Ci_8alkyl, hydroxyl-Ci^alkyl-amino, Cj-salkyl-thio, Ci-galkyl-carbonyl, Ci-8alkyl-carbonyl-oxy-Ci_8alkyl, Ci-galkoxy-carbonyl, C|_8alkyl-sulfonyl, Cs-ncycloalkyl, aryl-Ci-salkyl, aryl-amino, aryl-Ci.galky-amino, heteroaryl or heteroaryl-Ci .«alkyl, wherein heteroaryl and the aryl and heteroaryl portions of aryl-Ci.galkyl, aryl-amino, aryl-Ci_8alky-amino and heteroaryl-Ci.«alkyl are each optionally substituted with one, two, three or four halo or halo-Ci.galkoxy substituents.
Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from cyano, halo, hydroxyl, nitro, oxo, Ci^alkyl, cyano-Ci_«alkyl, halo-C 1-8alkyl, hydroxyl-C|.«alkyl, Cj .«alkoxy, Cj.«alkoxy-C|.«alkyl, halo-C|.«alkoxy, C2-8alkenyl, Ci_8alkoxy-C2-8alkenyl, C2_8alkynyl, Ci_8alkoxy-C2-8alkynyl, carboxyl, amino, Ci.galkyl-amino, (C].8alkyl)2-amino, amino-Ci.galkyl, C|.«alkyl-amino-Cj.«alkyl, (C].8alkyl)2-amino-Ci_8alkyl, hydroxyl-Ci_«alkyl-amino, hydroxyl-Ci.galkyl-amino-Ci-galkyl, hydroxyl-Ci-galkyl-amino-Ci.salkyl-amino, C|_«alkyl-thio, Cj.galkyl-carbonyl, Ci.galkyl-carbonyl-amino, Ci.galkyl-carbonyl-oxy, Ci.galkyl-carbonyl-oxy-Ci.galkyl, Ci-salkoxy-carbonyl, Ci.galkoxy-carbonyl-Ci.galkyl, C].8alkoxy-carbonyl-amino or C1 .«alkyl-sulfonyl.
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Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from cyano, halo, hydroxyl, nitro, Ci_«alkyl, cyano-Ci.« alkyl, halo-Ci-8alkyl, hydroxyl-Ci_«alkyl, C],.«alkoxy, Ci-8alkoxy-Ci.«alkyl, halo-Ci_8alkoxy, C2-8alkenyl, Ci.«alkoxy-C2-«alkenyl, carboxyl, amino, C].«alkyl-amino, Ci.«alkyl-amino-Ci.«alkyl, hydroxyl-Cj.salkyl-amino, C].«alkyl-thio, Ci_8alkyl-carbonyl, Ci.8alkyl-carbonyl-oxy-Ci-8alkyl, Ci-8alkoxy-carbonyl or C|.«alkyl-sulfonyl.
Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from optionally substituted C3_i4cycloalkyl selected from cyclopropyl or cyclobutyl; or, aryl, aryl-Cj.«alkyl, aryl-amino or aryl-Ci_«alky-amino optionally substituted on aryl and the aryl portions, wherein aryl is selected from phenyl; and, wherein the optional substituents on C3_i4cycloalkyl, aryl and the aryl portions are selected from one, two, three or four halo, Ci_«alkyl, halo-C i_«alkyl, hydroxyl-Ci.«alkyl, C].«alkoxy, halo-Ci.«alkoxy, hydroxyl-Ci-salkyl or carboxyl substituents; or, heteroaryl or heteroaryl-Ci_8alkyl optionally substituted on heteroaryl and the heteroaryl portion, wherein heteroaryl is selected from tetrazolyl or pyridinyl; and, wherein the optional substituents on heteroaryl and the heteroaryl portion are selected from one, two, three or four halo, Ci^alkyl, halo-C].«alkyl, hydroxyl-Ci.«alkyl, Ci.«alkoxy, halo-Ci_«alkoxy, hydroxyl-Ci_«alkyl or carboxyl substituents.
Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from optionally substituted C3_i4cycloalkyl selected from cyclopropyl or cyclobutyl; or, aryl-Ci.«alkyl, aryl-amino or aryl-Ci_«alky-amino optionally substituted on the aryl portions, wherein aryl is selected from phenyl; and, wherein the optional substituents on C3_i4cycloalkyl and the aryl portions are selected from one, two, three or four halo or halo-Ci.8alkoxy substituents; or, heteroaryl orheteroaryl-C|.«alkyl optionally substituted on heteroaryl and the heteroaryl portion, wherein heteroaryl is selected from tetrazolyl or pyridinyl; and, wherein the optional substituents on heteroaryl and the heteroaryl portion are selected from one, two, three or four halo or halo-Ci_«alkoxy substituents.
Another embodiment includes a compound of Formula (1), wherein R5 is independently selected from optionally substituted C3_i4cycloalkyl selected from cyclopropyl or cyclobutyl.
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Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from aryl, aryl-Ci-salkyl, aryl-amino or aryl-C|-«alky-amino optionally substituted on aryl and the aryl portions, wherein aryl is selected from phenyl; and, wherein the optional substituents are selected from one, two, three or four halo, Ci_8alkyl, halo-Ci_8alkyl, hydroxyl-Ci^alkyl, Ci-salkoxy, halo-Ci_«alkoxy, hydroxyl-C]_«alkyl or carboxyl substituents.
Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from aryl-Cj-xalkyl, aryl-amino or aryl-Ci-«alky-amino optionally substituted on the aryl portions, wherein aryl is selected from phenyl; and, wherein the optional substituents are selected from one, two, three or four halo or halo-Cj-salkoxy substituents.
Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from heteroaryl or heteroaryl-Ci-«alkyl optionally substituted on heteroaryl and the heteroaryl portion, wherein heteroaryl is selected from tetrazolyl or pyridinyl; and, wherein the optional substituents are selected from one, two, three or four halo, Ci-ealkyl, halo-C[-«alkyl, hydroxyl-Ci-salkyl, Ci^alkoxy, halo-Cj.«alkoxy, hydroxyl-C 1-8alkyl or carboxyl substituents.
Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from heteroaryl or hetcroaryl-C|-«alkyl optionally substituted on heteroaryl and the heteroaryl portion, wherein heteroaryl is selected from tetrazolyl or pyridinyl; and, wherein the optional substituents are selected from one, two, three or four halo or halo-Ci.galkoxy substituents.
Another embodiment includes a compound of Formula (I), wherein R5 is independently selected from heteroaryl or heteroaryl-Ci_salkyl optionally substituted on heteroaryl and the heteroaryl portion, wherein heteroaryl is selected from 2H-tetrazol-2-yl, tetrazol-1-yl, pyridin-2-yl, pyridin-3-yl or pyridin-4-yl; and, wherein the optional substituents are selected from one, two, three or four halo or halo-Ci_salkoxy substituents.
Another embodiment includes a compound of Formula (I), wherein R6 is independently selected from cyano, halo, hydroxyl, nitro, Ci.«alkyl, halo-C].«alkyl, hydroxyl-Ci-salkyl, C,-«alkoxy, halo-C|_«alkoxy, C2-salkenyl, C2-salkynyl, formyl, formyloxy, C].«alkyl-carbonyl, halo-C].«alkyl-carbonyl, Cj-salkyl-thio, halo-Ci_«alkyl-thio, amino,
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Cj-salkyl-carbonyl, Ci_8alkoxy-carbonyl, amino-carbonyl, C|_xalkyl-amino-carbonyl, amino-Ci.galkyl, (Ci.8alkyl)2-amino-Ci.8alkyl-amino, hydroxyl-C].8alkyl-amino, hydroxyl-imino-Cj-salkyl, Cj-salkyl-sulfonyl, B(OR8)2, C3_i4cycloalkyl, heterocyclyl, aryl or heteroaryl, wherein Cs-ucycloalkyl, heterocyclyl, aryl and heteroaryl are each optionally substituted with one, two, three or four halo or Ci_8alkyl substituents.
Another embodiment includes a compound of Formula (I), wherein R6 is independently selected from cyano, halo, hydroxyl, nitro, Ci_8alkyl, halo-Ci_8alkyl, hydroxyl-Ci_8alkyl, Ci_8alkoxy, halo-Ci_8alkoxy, C2_8alkenyl, Ci_8alkoxy-C2_8alkenyl, C2-8alkynyl, C].8alkoxy-C2-8alkynyl, carboxyl, formyl, formyl-oxy, Ci_8alkyl-carbonyl, halo-Ci_8alkyl-carbonyl, Ci_8alkyl-thio, halo-Ci_8alkyl-thio, amino, Ci_8alkyl-amino, (Ci_8alkyl)2-amino, C].8alkyl-carbonyl, Ci_8alkyl-carbonyl-oxy, Ci_8alkyl-carbonyl-oxy-Ci_8alkyl, Ci_8alkoxy-carbonyl, halo-Ci_8alkoxy-carbonyl, Ci_8alkoxy-carbonyl-Ci_8alkyl, Ci_8alkoxy-carbonyl-amino, Ci.8alkoxy-carbonyl-amino-Ci_8alkyl, amino-carbonyl, Ci_8alkyl-amino-carbonyl, (C].8alkyl)2-amino-carbonyl, Ci_8alkyl-carbonyl-amino, Ci_8alkyl-carbonyl-amino-Ci.8alkyl, amino-Ci.8alkyl, Ci_8alkyl-amino-Ci.8alkyl, (Ci_8alkyl)2-amino-Ci-8alkyl, arnino-Ci.8alkyl-amino, Ci.8alkyl-amino-Ci_8alkyl-amino, (Ci.8alkyl)2-amino-C].8alkyl-amino, hydroxyl-C].8alkyl-amino, hydroxyl-Ci.8alkyl-amino-C].8alkyl, hydroxyl-Ci.8alkyl-amino-Ci_8alkyl-amino, imino-Ci.8alkyl, hydroxyl-imino-Ci_8alkyl, Ci.8alkoxy-imino-Ci_8alkyl, C].8alkyl-sulfonyl, halo-Ci,8alkyl-sulfonyl, amino-sulfonyl, Ci_8alkyl-amino-sulfonyl, (Ci_8alkyl)2-amino-sulfonyl or B(OR8)2.
Another embodiment includes a compound of Formula (I), wherein R6 is independently selected from cyano, halo, hydroxyl, nitro, Ci_8alkyl, halo-Ci_8alkyl, hydroxyl-Ci_8alkyl, C].8alkoxy, halo-C].8alkoxy, C2_8alkenyl, C2_8alkynyl, formyl, formyloxy, C|.8alkyl-carbonyl, halo-Ci_8alkyl-carbonyl, Ci_8alkyl-thio, halo-Ci_8alkyl-thio, amino, Ci_8alkyl-carbonyl, Ci_8alkoxy-carbonyl, amino-carbonyl, Ci_8alkyl-amino-carbonyl, amino-C].8alkyl, (Ci_8alkyl)2-amino-Ch8alkyl-amino, hydroxyl-C]_8alkyl-amino, hydroxyl-imino-C].8alkyl, C].8alkyl-sulfonyl, Ci_8alkyl-amino-sulfonyl or B(OR8)2.
Another embodiment includes a compound of Formula (I), wherein Re is independently selected from C3_i4cycloalkyl, heterocyclyl, aryl or heteroaryl, wherein
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C3_i4cycloalkyl, heterocyclyl, aryl and heteroaryl are each optionally substituted with one, two, three or four halo or Ci-salkyl substituents.
Another embodiment includes a compound of Formula (I), wherein R.6 is independently selected from C3.i4cycloalkyl or heterocyclyl, wherein C3.i4cycloalkyl and heterocyclyl are each optionally substituted with two Chalky! substituents.
Another embodiment includes a compound of Formula (I), wherein R.6 optionally substituted C3.i4cycloalkyl is selected from cyclopropyl; optionally substituted heterocyclyl is selected from morpholinyl or 1,3,2-dioxaborolanyl; optionally substituted aryl is selected from phenyl; or, optionally substituted heteroaryl is selected from lH-pyrazolyl.
Another embodiment includes a compound of Formula (I), wherein R6 optionally substituted CvHcycloalkyl is selected from cyclopropyl.
Another embodiment includes a compound of Formula (I), wherein R6 optionally substituted heterocyclyl is selected from morpholinyl or 1,3,2-dioxaborolanyl.
Another embodiment includes a compound of Formula (I), wherein R6 optionally substituted heterocyclyl is selected from morpholin-4-yl or l,3,2-dioxaborolan-2-yl.
Another embodiment includes a compound of Formula (I), wherein R.6 optionally substituted aryl is selected from phenyl.
Another embodiment includes a compound of Formula (I), wherein R6 optionally substituted heteroaryl is selected from lH-pyrazolyl.
Another embodiment includes a compound of Formula (I), wherein R6 optionally substituted heteroaryl is selected from lH-pyrazol-l-yl.
Another embodiment includes a compound of Formula (I), wherein R7 is hydroxyl.
Another embodiment includes a compound of Formula (I), wherein R7 is (Ci.salkoxy)n, wherein n represents an integer from 1 to 5.
Another embodiment includes a compound of Formula (I), wherein R3 is hydrogen.
Another embodiment includes a compound of Formula (I), wherein Rs is Ci-salkyl.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a free acid, free base, salt, ester,
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Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a free acid, free base, salt, ester, hydrate, solvate or polymorph thereof.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a salt, ester, hydrate, solvate, chelate, clathrate, polymorph, isotopologue, stereoisomer, racemate, enantiomer, diastereomer or tautomer thereof.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a free acid, free base, salt, hydrate or polymorph thereof.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a free acid, free base, hydrate, solvate or polymorph thereof.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a salt, hydrate, solvate or polymorph thereof.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a free acid, free base or salt thereof.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a free acid or free base thereof.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a salt thereof.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is selected from a polymorph thereof.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is pharmaceutically acceptable.
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Another embodiment includes a compound of Formula (I) or a form thereof, wherein the form of the compound of Formula (I) is isolated.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the compound is a compound of Formula (II), Formula (III) or Formula (IV):
Figure AU2013348009C1_D0003
Formula (II), Formula (III) or Formula (IV) or a form thereof, wherein
R9 and Rio are independently hydrogen, hydroxyl, Cj-galkyl, hydroxyl-C|_8alkyl, Ci-salkoxy-Ci-salkyl, C|_8alkyl-carbonyl, amino-carbonyl, Ci^alkyl-amino-carbonyl, (Ci-8alkyl)2-amino-carbonyl, Ci-salkoxy-carbonyl, amino-sulfonyl, Ci_8alkyl-amino-sulfonyl, (Ci.8alkyl)2-amino-sulfonyl or P(O)(R7)2.
Another embodiment includes a compound of Formula (III), wherein one of R9 and
Rio is hydrogen and the other is hydroxyl, Ci-galkyl, hydroxyl-Ci.salkyl, Cj^alkoxy-Cpsalkyl, Ci-galkyl-carbonyl, amino-carbonyl, Ci^alkyl-amino-carbonyl, (Ci-8alkyl)2-amino-carbonyl, Ci-8alkoxy-carbonyl, amino-sulfonyl, C^alkyl-amino-sulfonyl, (Ci.8alkyl)2-amino-sulfonyl or P(O)(R7)2.
Another embodiment includes a compound of Formula (I) or a form thereof, wherein the compound is a compound of Formula (la), Formula (Ila), Formula (Illa) or Formula (IVa):
Figure AU2013348009C1_D0004
Figure AU2013348009C1_D0005
Figure AU2013348009C1_D0006
Figure AU2013348009C1_D0007
Formula (IVa)
Formula (la),
Formula (Ila),
Formula (Illa) or or a form thereof, wherein R2, R3, R9, Rio or Ri 1 are independently deuterium.
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Another embodiment includes a compound of Formula (I) or a form thereof selected from the group consisting of:
Figure AU2013348009C1_D0008
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Figure AU2013348009C1_D0009
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Figure AU2013348009C1_D0010
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Figure AU2013348009C1_D0011
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Figure AU2013348009C1_D0012
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Figure AU2013348009C1_D0013
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Figure AU2013348009C1_D0014
Figure AU2013348009C1_D0015
Figure AU2013348009C1_D0016
107
108
Figure AU2013348009C1_D0017
Figure AU2013348009C1_D0018
Figure AU2013348009C1_D0019
F
Figure AU2013348009C1_D0020
Figure AU2013348009C1_D0021
F
112
111
NH,
Figure AU2013348009C1_D0022
Figure AU2013348009C1_D0023
F
Figure AU2013348009C1_D0024
Figure AU2013348009C1_D0025
F
Figure AU2013348009C1_D0026
Figure AU2013348009C1_D0027
117
118
Figure AU2013348009C1_D0028
116
Figure AU2013348009C1_D0029
120
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Figure AU2013348009C1_D0030
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Figure AU2013348009C1_D0031
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Figure AU2013348009C1_D0032
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Figure AU2013348009C1_D0033
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Figure AU2013348009C1_D0034
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Figure AU2013348009C1_D0035
Figure AU2013348009C1_D0036
205
Figure AU2013348009C1_D0037
Figure AU2013348009C1_D0038
213
Figure AU2013348009C1_D0039
217
Figure AU2013348009C1_D0040
Figure AU2013348009C1_D0041
206
Figure AU2013348009C1_D0042
CN
210
Figure AU2013348009C1_D0043
Figure AU2013348009C1_D0044
214
Figure AU2013348009C1_D0045
Figure AU2013348009C1_D0046
218
Figure AU2013348009C1_D0047
Figure AU2013348009C1_D0048
Figure AU2013348009C1_D0049
Figure AU2013348009C1_D0050
Figure AU2013348009C1_D0051
Cl
219
Figure AU2013348009C1_D0052
208
Figure AU2013348009C1_D0053
Figure AU2013348009C1_D0054
Figure AU2013348009C1_D0055
Figure AU2013348009C1_D0056
F
216
Figure AU2013348009C1_D0057
Figure AU2013348009C1_D0058
cf3
220
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Figure AU2013348009C1_D0059
Figure AU2013348009C1_D0060
Figure AU2013348009C1_D0061
222
Figure AU2013348009C1_D0062
Figure AU2013348009C1_D0063
Figure AU2013348009C1_D0064
Figure AU2013348009C1_D0065
Figure AU2013348009C1_D0066
Figure AU2013348009C1_D0067
225
Figure AU2013348009C1_D0068
F
226
Figure AU2013348009C1_D0069
Figure AU2013348009C1_D0070
Figure AU2013348009C1_D0071
Figure AU2013348009C1_D0072
Figure AU2013348009C1_D0073
229
Figure AU2013348009C1_D0074
Figure AU2013348009C1_D0075
F
234
227
NH,
Figure AU2013348009C1_D0076
Figure AU2013348009C1_D0077
F
231
Figure AU2013348009C1_D0078
OyF
F
235
Figure AU2013348009C1_D0079
232
Figure AU2013348009C1_D0080
236
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ΝΗο
Figure AU2013348009C1_D0081
237 238
Figure AU2013348009C1_D0082
241 242
Figure AU2013348009C1_D0083
Figure AU2013348009C1_D0084
Figure AU2013348009C1_D0085
252
Figure AU2013348009C1_D0086
Figure AU2013348009C1_D0087
Figure AU2013348009C1_D0088
256
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Figure AU2013348009C1_D0089
257
Figure AU2013348009C1_D0090
258
Figure AU2013348009C1_D0091
Cl
261
Figure AU2013348009C1_D0092
Figure AU2013348009C1_D0093
265
Figure AU2013348009C1_D0094
266
Figure AU2013348009C1_D0095
Figure AU2013348009C1_D0096
Figure AU2013348009C1_D0097
Figure AU2013348009C1_D0098
268
Figure AU2013348009C1_D0099
Figure AU2013348009C1_D0100
269
Figure AU2013348009C1_D0101
Figure AU2013348009C1_D0102
273
Figure AU2013348009C1_D0103
274 275
Figure AU2013348009C1_D0104
276
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Figure AU2013348009C1_D0105
wherein the form of the compound of Formula (I) is selected from a salt, ester, hydrate, solvate, chelate, clathrate, polymorph, isotopologue, stereoisomer, racemate, enantiomer, diastereomer or tautomer thereof.
Another embodiment includes a compound of Formula (I) or a form thereof selected from the group consisting of:
Cpd Name
N-(4-methoxyphenyl)-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-amine N-(2,3-dihydro-1,4-benzodioxin-6-yl)-2~(2-methylimidazo[ 1,2-a]pyridin-3 - yl)pyrimidin-4-amine
2-(2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4-(trifhioromethyl)phenyl]pyrimidin-4- amine
N-(4-methoxyphenyl)-2-(2-methylimidazo[ 1,2-a]pyridin-3-yl)pyrimidin-4-amine
N-(4-chlorophenyl)-2-(2-methylimidazo[ 1,2-a]pyridin-3-yl)pyrimidin-4-amine
2-(2-methylimidazo[ 1,2-a]pyridin-3-yl)-N-phenylpyrimidin-4-amine
2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4- (trifluoromethyl)phenyl]pyrimidin-4-amine
N-(4-chlorophenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4- amine
N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4- amine
N-(4-bromophenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4- amine
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N-[4-(difluoromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine
N-(4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4- amine
2-[6-chloro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4- (trifluoromethyl)phenyl]pyrimidin-4-amine
2-[6-chloro-2-(trifluoromethyl)irnidazo[l,2-a]pyridin-3-yl]-N-[4- (trifluoromethoxy)phenyl]pyrimidin-4-amine N-(4-bromophenyl)-2-[6-chloro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine 2-[6-chloro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4- (difluoromethoxy)phenyl]pyrimidin-4-amine N-(4-chlorophenyl)-2-[6-chloro-2-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 - yl]pyrimidin-4-amine 2-[2-methyl-6-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4- (trifluoromethyl)phenyl]pyrimidin-4-amine
N-(4-bromophenyl)-2-[2-methyl-6-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine N-(4-methylphenyl)-2-[2-methyl-6-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine
2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-(4- methylphenyl)pyrimidin-4-amine
2-[6-fluoro-2-(trifluoromethyl)imidazo[ 1,2-a]pyridin-3-yl]-N-(4- methoxyphenyl)pyrimidin-4-amine
2-[5-chloro-l-methyl-2-(trifluoromethyl)-lH-indol-3-yl]-N-(4- methoxyphenyl)pyrimidin-4-amine
2-[5-chloro-l-methyl-2-(trifluoromethyl)-lH-indol-3-yl]-N-[4- (difluoromethoxy)phenyl]pyrimidin-4-amine
N-(4-bromophenyl)-2-[5-chloro-l-methyl-2-(trifluoromethyl)-lH-indol-3-yl]pyrimidin-
4-amine
N-(4-bromophenyl)-2-(6-fluoro-2-phenylimidazo[ 1,2-a]pyridin-3-yl)pyrimidin-4-amine
2-(6-fluoro-2-phenylimidazo[ 1,2-a]pyridin-3-yl)-N-(4-methylphenyl)pyrimidin-4-amine
N-(l,3-benzodioxol-5-yl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-
4-amine
N-(2,3-dihydro-l,4-benzodioxin-6-yl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine
N-(6-methoxypyridin-3-yl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-
4-amine
N2,N2-dimethyl-N5-{2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4- yl}pyridine-2,5-diamine
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2-[6-bromo-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4- (trifluoromethyl)phenyl]pyrimidin-4-amine
2-[6-bromo-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-(4- methoxyphenyl)pyrimidin-4-amine N-(3-fluoro-4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine N-(3-chloro-4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine
N-(3-chloro-4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine N-(4-ethoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4- amine
N-[4-(propan-2-yl)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-
4-amine
N- [4-( 1 H-pyrazol-1 -yl)phenyl] -2- [2-(trifluoromethyl)imidazo[ 1,2-a]pyridin-3 - yl]pyrimidin-4-amine
N-(3-chloro-4-methoxyphenyl)-2-(2-methyl-177-benzimidazol-l-yl)pyrimidin-4-amine
2-(2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidin-4-amine
N-(3-chloro-4-methoxyphenyl)-2-[2-(trifluoromethyl)-lH-benzimidazol-l- yl]pyrimidin-4-amine
5-fluoro-N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine
5-chloro-N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine N-(4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4- amine
2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]-N-[4- (trifluoromethyl)phenyl]pyrimidin-4-amine N-(4-chlorophenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4- amine
2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4- (trifluoromethyl)phenyl]pyrimidin-4-amine
2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4- (trifluoromethoxy )phenyl]pyrimidin-4-amine
N-(4-methoxyphenyl)-2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine N-[4-(difluoromethoxy)phenyl]-2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-
a]pyridin-3-yl]pyrimidin-4-amine
2-{[6-{[4-(difluoromethoxy)phenyl]amino}-2-(2-methyl-lH-benzimidazol-l- yl)pyrimidin-4-yI] amino} ethanol
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N-[4-(difluoromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3- yl]pyrimidin-4-amine 2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4- (trifluoromethyl)phenyl]pyrimidin-4-amine
N-[4-(difluoromethoxy)phenyl]-2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidin-4-amine
N-[4-(trifluoromethyl)phenyl]-2-[2-(trifluoromethyl)pyrazolo[l,5-a]pyridin-3- yl]pyrimidin-4-amine
2- {[2-(2-methyl-1 H-benzimidazol-1 -yl)-6- {[4- (trifluoromethyl)phenyl] amino } pyrimidin-4-yl] amino } ethanol N4-(2-methoxyethyl)-2-(2-methyl-1 H-benzimidazol-1 -yl)-N6-[4- (trifluoromethyl)phenyl]pyrimidine-4,6-diamine N4-[4-(difluoromethoxy)phenyl]-N6-(2-methoxyethyl)-2-(2-methyl-1 H-benzimidazol-1 - yl)pyrimidine-4,6-diamine N-(4-methoxyphenyl)-2-[2-(trifluoromethyl)pyrazolo[l,5-a]pyridin-3-yl]pyrimidin-4- amine
N-[4-(difluoromethoxy)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidin-4-amine
N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4- amine
2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6- diamine
2-(5,6-difluoro-2-methyl-l H-benzimidazol- l-yl)-N-[4- (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidine-4,6-diamine 2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4- (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(trifluoromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3- yl]pyrimidine-4,6-diamine 2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4- (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3- yl)pyrimidine-4,6-diamine
N-[4-(trifluoromethyl)phenyl]-2-( 1,3,5-trimethyl-1 H-pyrazol-4-yl)pyrimidine-4,6- diamine
2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(6-fluoro-2-methyl-l H-benzimidazol-1- yl)pyrimidine-4,6-diamine
2-(2-methyl- lH-imidazo[4,5-b]pyridin-l -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
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2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoroimidazo[l,2-a]pyridin-3-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-lyl)pyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]pyrimidine-4,6-diamine
N-[4-(trifluoromethyl)phenyl]-2-(2,5,6-trimethyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
N- [3 -fluoro-4-(trifluoromethyl)phenyl] -2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-
4,6-diamine
2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(2-cyclopropyl-6-fluoro-1 H-benzimidazol-1 -yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-5-fluoro-lH-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine [3-(4-amino-6-([4-(trifluoromethyl)phenyl]amino}pyrimidin-2-yl)-6fluoroimidazo [ 1,2-a]pyridin-2-yl]methanol
2-(6-bromo-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(2,6-dimethyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(6-ethyl-2-methyl- IH-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(4,6-difluoro-2 -methyl-1 H-benzimidazol-1 -yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-{[2-(4,6-difluoro-2-methyl-l H-benzimidazol-l-yl)-6-{[4(trifluoromethyl)phenyl] amino }pyrimidin-4-yl] amino} ethanol
2-(6-ethenyl-2-methyl-lH-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(6-fluoro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
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5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(6-chloro-2-methyl-l H-benzimidazol-1 -yl)-N-[3-fluoro-4- (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4- (difluoromethoxy)phenyl]pyrimidine-4,6-diamine
2-(5-chloro-2-methyl-l H-benzimidazol-l-yl)-N-[3-fluoro-4- (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(5-chloro-2-methyl-1 H-benzimidazol-1 -yl)-N-[4- (difluoromethoxy)phenyl]pyrimidine-4,6-diamine
2-(6-fluoro-2-methylimidazo[l,2-a]pyrimidin-3-yl)-N-[4-
100 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-
101 yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-
102 yl)pyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-
103 (difluoromethoxy)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-1 H-imidazo[4,5-b]pyridin-1 -yl)-N-[4-
104 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-ethyl-lH-imidazo[4,5-b]pyridin-l -yl)-N-[4-
105 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-lH-benzimidazol-l-
106 yl)pyrimidine-4,6-diamine
2-(2-ethyl-l H-benzimidazol-1 -yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
107 4,6-diamine
5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-
108 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1-yl)-N-[4-
109 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-
110 yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(6-fluoro-2-methyl-lH-
111 benzimidazol-1 -yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(5-fluoro-2-methyl-lH-
112 benzimidazol-1 -yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(5-fluoro-2-methyl-l H-benzimidazol-1-
113 yl)pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-5-fluoro-N-[4-
114 (trifluoromethyl )phenyl]pyrimidine-4,6-di amine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)phenyl]-
115 5-fluoropyrimidine-4,6-diamine
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2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)-3-
116 fluorophenyl]-5-fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-5-fluoro-N-[4-
117 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
118 2-(imidazo[ 1,2-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidin-4-amine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(2-methyl-lH-benzimidazol-l-
119 yl)pyrimidine-4,6-diamine
2-(2-cyclopropyl-l H-benzimidazol-l-yl)-5-fluoro-N-[4-
120 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-1 H-benzimidazol-1 -yl)-N-[4-(difluoromethoxy)phenyl]-5-
121 fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3-fluorophenyl]-5-
122 fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-
123 4,6-diamine N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)-5-
124 fluoropyrimidine-4,6-diamine 2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-
125 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-
126 yl)-5-fluoropyrimidine-4,6-diamine 2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-
127 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-
128 yl)-5-fluoropyrimidine-4,6-diamine 2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4-
129 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-4,6-difluoro-1 H-benzimidazol-1 -
130 yl)-5-fluoropyrimidine-4,6-diamine N-[4-(difluoromethoxy)phenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-
131 fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)-5-
132 fluoropyrimidine-4,6-diamine N-[4-(difluoromethoxy)phenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-
133 fluoropyrimidine-4,6-diamine 5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-
134 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol-l-
135 yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(4-fluoro-2-methyl-lH-
136 benzimidazol-1 -yl)pyrimidine-4,6-diamine
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5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-
137 (tri fluoromethyl)phenyl]pyrimidine-4,6-di amine N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-
138 yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(2-methyl-lH-imidazo[4,5-
139 b]pyridin-1 -yl)pyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4-
140 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5-
141 fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3-
142 fluorophenyl]-5-fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-l H-benzimidazol-l-yl)-N-[4-
143 (difluoromethoxy)phenyl]pyrimidine-4,6-diamine N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)pyrimidine-
144 4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-[2-(difluoromethyl)-6-fluoro-lH-benzimidazol-l-
145 yl]pyrimidine-4,6-diamine
2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(methylsulfanyl)phenyl]pyrimidine-4,6-
146 diamine
2-[2-( 1-methyl cyclopropyl)-1 H-benzimidazol-1-yl]-N-[4-
147 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-[2-(l-methylcyclopropyl)-lH-benzimidazol-l-
148 yl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-
149 diamine
2-[2-(methoxymethyl)-l H-benzimidazol-l-yl]-N-[4-
150 (trifluoromethyl)phenyl]pyrimidme-4,6-diamine
2-[2-(propan-2-yl)-1 H-benzimidazol-1 -yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-
151 4,6-diamine
2-[2-(difluoromethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-
152 4,6-diamine
2-(2-ethyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-
153 diamine
2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-
154 diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-
155 (difluoromethoxy)phenyl]-5-fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)pyrimidine-4,6-
156 diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)pyrimidine-
157 4,6-diamine
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2-(5-chloro-2-methyl-l H-benzimidazol-1-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
2-(6-chloro-2-methyl-l H-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-l H-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
2-(2-ethyl-5-fluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-5-fluoro-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
2-(2-ethyl-6-fluoro-1 H-benzimidazol-1 -yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamme
5-chloro-2-(2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
5-chloro-2-(2-ethyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
5-chloro-N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)pyrimidine-
4,6-diamine
5-fluoro-2-(2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methylimidazo[l,2-a]pyridin-3yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(2-methylimidazo[ 1,2-a]pyridin-3yl)pyrimidine-4,6-diamine
-methyl-2-(2-methyl-1 H-benzimidazol-1 -yl)-N- [4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methylpyrazolo[l,5-a]pyridin-3yl)pyrimidine-4,6-diamine
5-fluoro-N-[4-(trifluoromethyl)phenyl]-2-(2,6,8-trimethylimidazo[l,2-a]pyrazin-3yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2,6,8-trimethylimidazo[l,2-a]pyrazin-3yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(2,6,8-trimethylimidazo[l,2a]pyrazin-3-yl)pyrimidine-4,6-diamine
5-fluoro-2-(2-methylpyrazolo[ 1,5-a]pyridin-3-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-fluoro-2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
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5-fluoro-2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-
179 4,6-diamine
2-(2-cyclopropylpyrazolo[l,5-a]pyridin-3-yl)-N-[4-(difluoromethoxy)phenyl]-5-
180 fluoropyrimidine-4,6-diamine [3-(4-amino-6-{[4-(difluoromethoxy)phenyl]amino}-5-fluoropyrimidin-2-yl)-5-
181 fluoropyrazolo[l ,5-a]pyridin-2-yl]methanol
2-[2-(methylsulfanyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-
182 4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1-yl)-N-[6-(trifluoromethyl)pyridin-3 -
183 yl]pyrimidine-4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)-N-(4-methylphenyl)pyrimidine-
184 4,6-diamine
N-(4-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
185 4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-5-fluoropyrazolo[l,5-a]pyridin-3-yl)-5-
186 fluoropyrimidine-4,6-diamine
2-(2-ethyl-5-fluoropyrazolo[l ,5-a]pyridin-3-yl)-5-fluoro-N-[4-
187 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-5-fluoropyrazolo[l,5-a]pyridin-3-
188 yl)-5-fluoropyrimidine-4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(3-methoxyphenyl)pyrimidine-
189 4,6-diamine
N-(3-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-
190 4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-
191 (trifluoromethoxy)phenyl]pyrimidine-4,6-diamine
4- {[6-amino-5-fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-
192 yl]amino}benzonitrile methyl 4-{[6-amino-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidin-4-
193 yl]amino}benzoate
5- fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-(3-methylphenyl)pyrimidine-4,6-
194 diamine
5-fluoro-N-(3-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-
195 diamine
196 2-(2-methyl-1 H-benzimidazol-1 -yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
197 N-(4-methoxyphenyl)-2-(2-methyl-1 H-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-[4-(dimethylamino)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-
198 diamine
5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-
199 diamine
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5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-
200 diamine N-(4-chlorophenyl)-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-
201 diamine
4- {[6-amino-5-fluoro-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-
202 yl] amino} benzonitrile
N-(l,3-benzodioxol-5-yl)-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-
203 diamine
5- fluoro-2-(2-methyl-1 H-benzimidazol-l-yl)-N-[4-
204 (trifluoromethoxy)phenyl]pyrimidine-4,6-diamine
205 N-(l ,3-benzodioxol-5-yl)-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6-diamine
N-(2,2-difluoro-l,3-benzodioxol-5-yl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-
206 4,6-diamine
N-(3-fluoro-4-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-
207 diamine
208 N-(6-methoxypyridin-3-yl)-2-(2-methyl-1 H-benzimidazol-1-yl)pyrimidine-4,6-diamine
209 N-(4-chlorophenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
210 4- {[6-amino-2-(2 -methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-yl] amino} benzonitrile
211 2-(2-methyl-1 H-benzimidazol-1 -yl)-N-(4-nitrophenyl)pyrimidine-4,6-diamine
212 N-(4-bromophenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-
213 methylphenyl)pyrimidine-4,6-diamine
2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-
214 methoxyphenyl)pyrimidine-4,6-diamine
N-(4-chlorophenyl)-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-
215 fluoropyrimidine-4,6-diamine N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-
216 yl]pyrimidine-4,6-diamine
5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-(4-methylphenyl)pyrimidine-
217 4,6-diamine
5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-(4-
218 methoxyphenyl)pyrimidine-4,6-diamine
N-(4-chlorophenyl)-5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]pyrimidine-
219 4,6-diamine
5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-[4-
220 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6-
221 diamine l-(4-amino-5-fluoro-6-{[4-(trifluoromethyl)phenyl]amino}pyrimidin-2-yl)-2-methyl-
222 1 H-benzimidazol e-6-carbonitrile
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-(4-amino-6- {[4-(difluoromethoxy)phenyl] amino} -5-fluoropyrimidin-2-yl)-2-methyl1 H-benzimidazole-6-carbonitrile l-{4-amino-5-fluoro-6-[(4-methylphenyl)amino]pyrimidin-2-yl}-2-methyl-lHbenzimidazole-6-carbonitrile l-{4-amino-5-fluoro-6-[(4-methoxyphenyl)amino]pyrimidin-2-yl}-2-methyl-lHbenzimidazole-6-carbonitrile l-(4-amino-6-{[4-(difluoromethoxy)phenyl]amino}-5-fluoropyrimidin-2-yl)-2-methyl1 H-benzimidazole-5-carbonitrile
- {4-amino-5-fluoro-6-[(4-methylphenyl)amino]pyrimidin-2-yl} -2-methyl-1Hbenzimidazole-5-carbonitrile
- {4-amino-5-fluoro-6-[(4-methoxyphenyl)amino]pyrimidin-2-yl} -2-methyl-1Hbenzimidazole-5-carbonitrile
1- (4-amino-5-fluoro-6-{[4-(trifluoromethyl)phenyl]amino}pyrimidin-2-yl)-2-methyl-
H-benzimidazole-5-carbonitrile
- {4-amino-6-[(4-chlorophenyl)amino]-5-fluoropyrimidin-2-yl} -2-methyl- 1Hbenzimidazole-5-carbonitrile
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-6-nitro-lH-benzimidazol-lyl)pyrimidine-4,6-diamine
5-fluoro-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-
4,6-diamine
5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-methyl-1 H-benzimidazol-1yl)pyrimidine-4,6-diamine
5-fluoro-2-(2-methyl-6-nitro-l H-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-(4-chlorophenyl)-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
2- (4,6-difluoro-2-methyl-1 H-benzimidazol-l-yl)-5-fluoro-N-[4- (trifluoromethoxy)phenyl ] pyrimidine-4,6 - di amine 5-fluoro-N-(4-methoxyphenyl)-2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)pyrimidine-4,6diamine
N-(l,3-benzodioxol-5-yl)-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4methylphenyl)pyrimidine-4,6-diamine
2-(4,6-difluoro-2 -methyl-1 H-benzimidazol-1 -yl)-5-fluoro-N-(4methoxyphenyl)pyrimidine-4,6-diamine
2-(5,7-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
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5-fluoro-2-(6-methoxy-2-methyl-l H-benzimidazol-l-yl)-N-[4-
244 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine N-(4-chlorophenyl)-5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-
245 yl)pyrimidine-4,6-diamine
5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-[4-
246 (trifluoromethoxy)phenyl]pyrimidine-4,6-diamine N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-
247 yl)pyrimidine-4,6-diamine
5-fluoro-2-(6-methoxy-2-methyl-1 H-benzimidazol-1 -yl)-N-(4-
248 methylphenyl)pyrimidine-4,6-diamine
5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-(4-
249 methoxyphenyl)pyrimidine-4,6-diamine
N-( 1,3-benzodioxol-5-yl)-5-fluoro-2-(6-methoxy-2-methyl-1 H-benzimidazol-1 -
250 yl)pyrimidine-4,6-diamine N-(4-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-
251 yl)pyrimidine-4,6-diamine
5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4-
252 methoxyphenyl)pyrimidine-4,6-diamine
5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4-
253 methylphenyl)pyrimidine-4,6-diamine
5-fluoro-2-(2-methyl-5-nitro-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-
254 4,6-diamine
5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-5-nitro-1 H-benzimidazol-1 -yl)pyrimidine-
255 4,6-diamine
2-(6-amino-2-methyl-l H-benzimidazol-l-yl)-5-fluoro-N-(4-
256 methoxyphenyl)pyrimidine-4,6-diamine
2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5-
257 fluoropyrimidine-4,6-diamine
2-(6-amino-2-methyl-lH-bcnzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-
258 4,6-diamine
N-(4-chlorophenyl)-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
259 4,6-diamine
N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(5-fluoro-2-methyl-l H-benzimidazol-1-
260 yl)pyrimidine-4,6-diamine
N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-
261 4,6-diamine
N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-
262 yl)pyrimidine-4,6-diamine
N-(4-chlorophenyl)-2-(6-fluoro-2-methyl-l H-benzimidazol-1-yl)pyrimidine-4,6-
263 diamine
2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-
264 diamine
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2-(6-fhioro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6-
265 diamine N-[4-(dimethylamino)phenyl]-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
266 4,6-diamine N-(4-chloro-3-fluorophenyl)-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
267 4,6-diamine
2-(6-fluoro-2-methyl- 1 H-benzimidazol-1 -yl)-N-(3 -methylphenyl)pyrimidine-4,6-
268 diamine
N-(2,2-difluoro-l,3-benzodioxol-5-yl)-2-(6-fluoro-2-methyl-lH-benzimidazol-l-
269 yl)pyrimidine-4,6-diamine
270 2-(2-ethyl-1 H-benzimidazol-1 -yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine 2-(2-ethyl-1 H-benzimidazol-1 -yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-
271 diamine
2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethoxy)phenyl]pyrimidine-
272 4,6-diamine
N-(l,3-benzodioxol-5-yl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-
273 diamine
274 N-(4-chlorophenyl)-2-(2-ethyl-l H-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine N-(4-chloro-3-fluorophenyl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-
275 diamine
2-(2-cyclopropyl-l H-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-
276 diamine
2-(2-cyclopropyl-1 H-benzimidazol-1 -yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-
277 diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-
278 (trifluoromethoxy)phenyl]pyrimidine-4,6-diamine N-(4-chlorophenyl)-2-(2-cyclopropyl-l H-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-
279 diamine
N-(4-chloro-3-fluorophenyl)-2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-
280 fluoropyrimidine-4,6-diamine
5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-
281 4,6-diamine
5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-
282 4,6-diamine
5-fhioro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-
283 (trifluoromethoxy)phenyl]pyrimidine-4,6-diamine, and
2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-
284 (trifluoromethyl)phenyl]pyrimidine-4,6-diamine;
wherein the form of the compound of Formula (I) is selected from a salt, ester, hydrate, solvate, chelate, clathrate, polymorph, isotopologue, stereoisomer, racemate, enantiomer, diastereomer or tautomer thereof.
47a
2013348009 09 Apr 2019
In a first aspect of the present invention there is provided a compound of Formula (I):
Figure AU2013348009C1_D0106
or a form thereof, wherein
Ri is bicyclic heteroaryl or bicyclic heterocyclyl substituted on a carbon atom ring member with one, two, three or four Rs substituents, or on a nitrogen atom ring member with an oxygen atom substituent to form an N-oxide;
X is N or N substituted with an oxygen atom substituent to form an N-oxide;
R2 is amino;
R3 is hydrogen, cyano, halo, Ci-salkyl, amino, Ci-salkyl-amino or (Ci-8alkyl)2-amino;
R4 is phenyl, optionally substituted with one, two, three or four Re substituents;
Rs is independently selected from the group consisting of cyano, halo, hydroxyl, nitro, oxo,
Ci-8alkyl, cyano-Ci-8alkyl, halo-Ci-8alkyl, hydroxyl-Ci-8alkyl, Ci-8alkoxy, Ci-salkoxy-Ci-salkyl, halo-Ci-8alkoxy, C2.8alkenyl, Ci-8alkoxy-C2-8alkenyl, C2-8alkynyl, Ci-8alkoxy-C2-8alkynyl, carboxyl, amino, Ci-salkyl-amino, (Ci-8alkyl)2-amino, amino-Ci-8alkyl, Ci-salkyl-amino-Ci-salkyl, (Ci-8alkyl)2-amino-Ci-8alkyl, hydroxyl-C 1 -salkyl-amino, hydroxyl-C 1 -salkyl-amino-C 1 -salkyl, hydroxyl-Ci-salkyl-amino-Ci-salkyl-amino, Ci-salkyl-thio, Ci-8alkyl-carbonyl, Ci-8alkyl-carbonyl-amino, Ci-8alkyl-carbonyl-oxy, Ci-salkyl-carbonyl-oxy-Ci-salkyl, C1 -salkoxy-carbonyl, C1.8alkoxy-carbonyl-C 1 -salkyl, C1 -salkoxy-carbonyl-amino, Ci-8alkyl-sulfonyl, C3-i4cycloalkyl, aryl, aryl-Ci-8alkyl, aryl-amino, aryl-Ci-salky-amino, heteroaryl, heteroaryl-Ci-8alkyl and heterocyclyl, wherein C3-i4cycloalkyl, aryl, heteroaryl or heterocyclyl and the aryl and heteroaryl portions of aryl-Ci-8alkyl, aryl-amino, aryl-Ci-salky-amino and heteroaryl-Ci-8alkyl are each optionally substituted with one, two, three or four halo, Ci-8alkyl, halo-Ci-8alkyl, hydroxyl-Ci-8alkyl, Ci-8alkoxy, halo-Ci-8alkoxy, hydroxyl-Ci-8alkoxy or carboxyl substituents;
Re is independently selected from the group consisting of cyano, halo, nitro, Ci-8alkyl, halo-Ci-8alkyl, hydroxyl-Ci-8alkyl, Ci-8alkoxy, halo-Ci-8alkoxy, C2.8alkenyl,
AH26( 13743554 1 ):MXC
47b
2013348009 19 Oct 2017
Ci_8alkoxy-C2-8alkenyl, C2-8alkynyl, Ci_8alkoxy-C2-salkynyl, carboxyl, formyl, formyloxy, Ci.salkyl-carbonyl, halo-C i-salkyl-carbonyl, Ci-salkyl-thio, halo-C i-salkyl-thio, amino, Ci-salkyl-amino, (Ci-salkyl-amino, C i-salkyl-carbonyl, Ci-salkyl-carbonyl-oxy, C i _8alkyl-carbonyl-oxy-C 1 -salkyl, C1 .salkoxy-carbonyl, halo-C 1 .salkoxy-carbonyl, Ci_8alkoxy-carbonyl-Ci_8alkyl, Ci-salkoxy-carbonyl-amino, Ci.salkoxy-carbonyl-amino-Cl.salkyl, amino-carbonyl, Ci-salkyl-amino-carbonyl, (Ci_8alkyl)2-amino-carbonyl, Ci-salkyl-carbonyl-amino, Ci.salkyl-carbonyl-amino-Cl.salkyl, amino-Ci-salkyl, Ci-salkyl-amino-Ci.salkyl, (C i _8alkyl)2-amino-C 1 -salkyl, amino-C 1 .salkyl-amino, C1 .salkyl-amino-C 1 .salkyl-amino, (Ci_8alkyl)2-amino-Ci.salkyl-amino, hydroxyl-Ci.salkyl-amino, hydroxyl-Ci.8alkyl-amino-Ci.8alkyl, hydroxyl-Ci.salkyl-amino-Ci.salkyl-amino, imino-C i -salkyl, hydroxyl-imino-C i -salkyl, C i .salkoxy-imino-C i -salkyl, Ci_8alkyl-sulfonyl, halo-Ci_salkyl-sulfonyl, amino-sulfonyl, Ci-salkyl-amino-sulfonyl, (Ci_8alkyl)2-amino-sulfonyl, B(ORs)2, C3-i4cycloalkyl, heterocyclyl, aryl and heteroaryl, wherein C3_i4cycloalkyl, heterocyclyl, aryl, and heteroaryl are each optionally substituted with one, two, three or four halo or Ci-salkyl substituents; and
Rs is independently hydrogen or Ci.salkyl;
wherein the form of the compound is selected from the group consisting of a free acid, free base, salt, ester, hydrate, solvate, isotopologue, stereoisomer, racemate, enantiomer, diastereomer and tautomer thereof.
In a second aspect of the present invention there is provided a compound or form thereof of the first aspect, selected from the group consisting of: 2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(5,6-difhioro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine N-[4-(difhioromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidine-4,6diamine 2-[2-(trifhioromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine N-[4-(trifhioromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidine-4,6diamine 2-(6-fhioro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
AH26( 13743554 1 ):MXC
47c
2013348009 15 Jun 2017
N-[4-(difluoromethoxy)phenyl]-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6diamine
N-[4-(trifluoromethyl)phenyl]-2-(l,3,5-trimethyl-lH-pyrazol-4-yl)pyrimidine-4,6-diamine 2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(2-cyclopropyl-6-fluoroimidazo[l,2-a]pyridin-3-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
2-(2-cyclopropyl-6-fluoro-1 H-benzimidazol-1 -yl)-N- [4-(difluoromethoxy)-3 fluorophenyl]pyrimidine-4,6-diamine
N-[4-(trifluoromethyl)phenyl]-2-(2,5,6-trimethyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-[3-fluoro-4-(trifluoromethyl)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(2-cyclopropyl-6-fluoro-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(2-cyclopropyl-5-fluoro-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine [3-(4-amino-6-{[4-(trifluoromethyl)phenyl]amino}pyrimidin-2-yl)-6-fluoroimidazo[ 1,2-a]pyridin2-yl] methanol
2-(6-bromo-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2,6-dimethyl-l H-benzimidazol- l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(6-ethyl-2-methyl-l H-benzimidazol- l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(4,6-difluoro-2-methyl-1 H-benzimidazol- l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(6-ethenyl-2-methyl-l H-benzimidazol- l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
13102725v2
47d
2013348009 15 Jun 2017
2-(6-fluoro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-1 H-benzimidazol-1 -yl)-N-[3 -fluoro-4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine-4,6diamine
2-(5 -chloro-2-methyl-1 H-benzimidazol-1 -yl)-N-[3 -fluoro-4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine-4,6diamine
2-(6-fluoro-2-methylimidazo[l,2-a]pyrimidin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl] -2-(5,6-difluoro-2-methyl-l H-benzimidazol- l-yl)pyrimidine-4,6diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(difluoromethoxy)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(6-chloro-2-ethyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl] -5-fluoro-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6diamine
2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl] -5-fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6 -diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6 -diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
13102725v2
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2013348009 15 Jun 2017
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
2-(6-chloro-2-methyl-1 H-imidazo [4,5 -b]pyridin-1 -yl)-N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-1 H-imidazo [4,5 -b]pyri din-1 -y 1) - 5 -fluoro-N- [4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(2-methyl-l H-benzimidazol- l-yl)pyrimidine-
4,6-diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5-fluoropyrimidine-4,6diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3-fluorophenyl]-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl] -2-(2-ethyl-1 H-benzimidazol-1 -yl)-5-fhioropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
2-(5,6-difhroro-2-methyl-lH-benzimidazol-l-yl)-5-fhioro-N-[4-(trifhioromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
2-(4,6-difhioro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
2-(2-ethyl-4,6-difluoro-1 H-benzimidazol-1 -yl)-5-fhioro-N-[4-(trifhioromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)-5-fluoropyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl] -2-(5,6-difluoro-2-methyl-1 H-benzimidazol-1 -yl)-5 fLuoropyrimidine-4,6-diamine
5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl] -5-fluoro-2-(4-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6 -diamine
13102725v2
47f
2013348009 15 Jun 2017
5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridin-lyl)pyrimidine-4,6 -diamine
2-(2-cyclopropyl-4-fluoro-1 H-benzimidazol-1 -yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-1 H-benzimidazol-1 -yl)-N- [4-(difluoromethoxy)phenyl] -5 fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-1 H-benzimidazol-1 -yl)-N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-6-fluoro-l H-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl] -2-[2-(difluoromethyl)-6-fluoro-1 H-benzimidazol-1 -yl]pyrimidine-
4,6-diamine
2-(2-methyl-l H-benzimidazol-l-yl)-N-[4-(methylsulfanyl)phenyl]pyrimidine-4,6-diamine
2-[2-(l -methylcyclopropyl)-1 H-benzimidazol- l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl] -2-[2-( 1 -methylcyclopropyl)-1 H-benzimidazol-1 -yl]pyrimidine-4,6diamine
2-(2-cyclopropyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-[2-(methoxymethyl)-l H-benzimidazol- l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-[2-(propan-2-yl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-[2-(difluoromethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-ethyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl] -2-(2-ethyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6-diamine N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(5 -chloro-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(difluoromethoxy)phenyl] -5 -fluorop yrimidine-
4,6-diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
13102725v2
2013348009 15 Jun 2017
47g
2-(6-chloro-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(difluoromethoxy)phenyl] -5 -fluorop yrimidine-
4,6-diamine
2-(2-ethyl-5-fluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-5-fluoro-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
5-chloro-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 5-chloro-2-(2-ethyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 5-chloro-N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 5-fluoro-2-(2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6diamine
N-[4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(2-methylimidazo [ 1,2-a]pyridin-3 yl)pyrimidine-4,6 -diamine
5-methyl-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifhioromethyl)phenyl]pyrimidine-4,6-diamine N-[4-(difhioromethoxy)phenyl]-5-fluoro-2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)pyrimidine-4,6diamine
5-fhioro-N-[4-(trifhioromethyl)phenyl]-2-(2,6,8-trimethylimidazo[l,2-a]pyrazin-3-yl)pyrimidine-
4,6-diamine
N-[4-(difhioromethoxy)phenyl]-5-fhioro-2-(2,6,8-trimethylimidazo[l,2-a]pyrazin-3-yl)pyrimidine-
4,6-diamine
N-[4-(difhioromethoxy)-3-fluorophenyl]-5-fluoro-2-(2,6,8-trimethylimidazo[l,2-a]pyrazin-3yl)pyrimidine-4,6-diamine
5-fhroro-2-(2-methylpyr azolof l,5-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
5-fhioro-2-[6-fhioro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-fhioro-2-(6-fhioro-2-methyl-lH-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6-diamine
2-(2-cyclopropylpyrazolo [1,5 -a]pyridin-3 -yl)-N-[4-(difhioromethoxy)phenyl] -5 -fluorop yrimidine-
4,6-diamine [3 -(4-amino-6- {[4-(difluoromethoxy)phenyl] amino } -5 -fluorop yrimidin-2-yl)-5 -fluorop yrazolo [1,5a]pyridin-2-yl] methanol
2-[2-(methylsulfanyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-fhioro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)-N-[6-(trifluoromethyl)pyridin-3 yl]pyrimidine-4,6-diamine
13102725v2
47h
2013348009 15 Jun 2017
5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
N-(4-chlorophenyl)-5 -fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-5-fluoropyrazolo[l,5-a]pyridin-3-yl)-5fluoropyrimidine-4,6-diamine
2-(2-ethyl-5 -fluorop yrazolo [1,5 -a]pyridin-3 -y 1)-5 -fluoro-N- [4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-5-fluoropyrazolo[l,5-a]pyridin-3-yl)-5fluoropyrimidine-4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(3-methoxyphenyl)pyrimidine-4,6-diamine N-(3-chlorophenyl)-5 -fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6-diamine 5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-
4,6-diamine
4- {[6-amino-5-fluoro-2-(6-fluoro-2-methyl-l H-benzimidazol-1 -yl)pyrimidin-4- yl] amino (benzonitrile methyl 4- {[6-amino-5 -fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4yl] amino (benzoate
5- fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-(3-methylphenyl)pyrimidine-4,6-diamine 5-fluoro-N-(3-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(2-methyl-l H-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
N-(4-methoxyphenyl)-2-(2-methyl-l H-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-[4-(dimethylamino)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine 5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-(4-chlorophenyl)-5-fluoro-2-(2-methyl-1 H-benzimidazol- l-yl)pyrimidine-4,6-diamine
4- {[6-amino-5 -fluoro-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-yl] amino ( benzonitrile
5- fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6diamine
N-(3-fluoro-4-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-(4-chlorophenyl)-2-(2-methyl-l H-benzimidazol-l-yl)pyrimidine-4,6-diamine
4- {[6-amino-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-yl] amino (benzonitrile
2-(2-methyl-l H-benzimidazol-l-yl)-N-(4-nitrophenyl)pyrimidine-4,6-diamine N-(4-bromophenyl)-2-(2-methyl-l H-benzimidazol-l-yl)pyrimidine-4,6-diamine
2-(5,6-difluoro-2 -methyl- lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine -4,6diamine
2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
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N-[4-(difluoromethoxy)phenyl] -5-fluoro-2-[2-(methoxymethyl)-1 H-benzimidazol-1 -yl]pyrimidine-
4,6-diamine
5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-(4-methylphenyl)pyrimidine-4,6-diamine 5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-(4-methoxyphenyl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-5 -fluoro-2-[2-(methoxymethyl)-1 H-benzimidazol-1 -yl]pyrimidine-4,6-diamine
5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine
-(4-amino-5-fluoro-6- {[4-(trifluoromethyl)phenyl] amino } pyrimidin-2-yl)-2-methyl- 1Hbenzimidazole-6-carbonitrile
-(4-amino-6- {[4-(difluoromethoxy)phenyl] amino } -5 -fluorop yrimidin-2-yl)-2-methyl-1Hbenzimidazole-6-carbonitrile
- {4-amino-5-fluoro-6-[(4-methylphenyl)amino]pyrimidin-2-yl} -2-methyl-1 H-benzimidazole-6carbonitrile l-{4-amino-5-fluoro-6-[(4-methoxyphenyl)amino]pyrimidin-2-yl}-2-methyl-lH-benzimidazole-6carbonitrile
-(4-amino-6- {[4-(difluoromethoxy)phenyl] amino } -5 -fluorop yrimidin-2-yl)-2-methyl-1Hbenzimidazole-5-carbonitrile
- {4-amino-5-fluoro-6-[(4-methylphenyl)amino]pyrimidin-2-yl} -2-methyl- lH-benzimidazole-5carbonitrile
1- {4-amino-5-fhioro-6-[(4-methoxyphenyl)amino]pyrimidin-2-yl}-2-methyl-lH-benzimidazole-5carbonitrile
-(4-amino-5-fluoro-6- {[4-(trifluoromethyl)phenyl] amino } pyrimidin-2-yl)-2-methyl- 1Hbenzimidazole-5-carbonitrile
- {4-amino-6- [(4-chlorophenyl)amino] -5 -fluoropyrimidin-2-yl} -2-methyl-1 H-benzimidazole-5 carbonitrile
N-[4-(difluoromethoxy)phenyl] -5-fluoro-2-(2-methyl-6-nitro-1 H-benzimidazol-1 -yl)pyrimidine-
4,6-diamine
5-fluoro-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
5-fhioro-N-(4-methoxyphenyl)-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-[4-(difhioromethoxy)phenyl]-2-(2-methyl-1 H-benzimidazol- l-yl)pyrimidine-4,6-diamine N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
5-fhioro-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-(4-chlorophenyl)-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
2- (4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine
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5-fluoro-N-(4-methoxyphenyl)-2-(2-methylpyr azolof l,5-a]pyridin-3-yl)pyrimidine-4,6-diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6diamine
2-(5,7-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
5-fluoro-2-(6-methoxy-2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-(4-chlorophenyl)-5 -fluoro-2-(6-methoxy-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6diamine
5-fluoro-2-(6-methoxy-2-methyl-l H-benzimidazol-1 -yl)-N-[4(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine
5-fluoro-2-(6-methoxy-2-methyl-l H-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6diamine
5-fluoro-2-(6-methoxy-2-methyl-l H-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6diamine
5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4-methoxyphenyl)pyrimidine-4,6diamine
5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4-methylphenyl)pyrimidine-4,6diamine
5-fluoro-2-(2-methyl-5-nitro-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-5-nitro-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6diamine
2-(6-amino-2-methyl-1 H-benzimidazol-1 -yl)-N- [4-(difluoromethoxy)phenyl] -5 -fluoropyrimidine-
4,6-diamine
2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine N-(4-chlorophenyl)-5 -fluoro-2-(5 -fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6-diamine N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)pyrimidine-4,6-diamine
2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
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2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6-diamine
N-[4-(dimethylamino)phenyl]-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-(4-chloro-3-fluorophenyl)-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(3-methylphenyl)pyrimidine-4,6-diamine
2-(2-ethyl-l H-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine
2-(2-ethyl-l H-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-diamine
2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine
N-(4-chlorophenyl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine
N-(4-chloro-3-fluorophenyl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-diamine 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6diamine
N-(4-chlorophenyl)-2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine
N-(4-chloro-3-fluorophenyl)-2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6-diamine
5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-
4,6-diamine, and,
2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine, wherein the form of the compound is selected from the group consisting of a free acid, free base, salt, ester, hydrate, solvate, isotopologue, stereoisomer, racemate, enantiomer, diastereomer and tautomer thereof.
In a third aspect of the present invention there is provided a pharmaceutical composition comprising a compound according to the first aspect or a form thereof in admixture with a pharmaceutically acceptable excipient.
In a fourth aspect of the present invention there is provided a pharmaceutical composition comprising a compound according to the second aspect or a form thereof in admixture with a pharmaceutically acceptable excipient.
In a fifth aspect of the present invention there is provided a method of inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising administering to the subject an effective amount of the compound of the first or second aspect or a form thereof.
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In a sixth aspect of the present invention there is provided use of the compound of first or second aspect or a form thereof in the manufacture of a medicament for inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising administering an effective amount of the medicament to the subject.
In a seventh aspect of the present invention there is provided a method of inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising administering to the subject an effective amount of the compound of the second aspect or a form thereof.
In an eighth aspect of the present invention there is provided a use of the compound or form thereof of the second aspect in the manufacture of a medicament for inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising administering an effective amount of the medicament to the subject.
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Terminology
The chemical terms used above and throughout the description herein, unless specifically defined otherwise, shall be understood by one of ordinary skill in the art to have the following indicated meanings.
As used herein, the term “Ci_8alkyl” refers to saturated hydrocarbon radicals having from one to eight carbon atoms in a straight or branched chain configuration, including, without limitation, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl and the like. In some embodiments, Chalky! includes Ci_6alkyl, Ci_4alkyl and the like. A Cj.salkyl radical may be optionally substituted where allowed by available valences.
As used herein, the term “C2_8alkenyl” refers to partially unsaturated hydrocarbon radicals having from two to eight carbon atoms in a straight or branched chain configuration and one or more carbon-carbon double bonds therein, including, without limitation, ethenyl, allyl, propenyl and the like. In some embodiments, C2_8alkenyl includes C2.6alkcnyl, C2.4alkenyl and the like. A C2_8alkenyl radical may be optionally substituted where allowed by available valences.
As used herein, the term “C2.8alkynyl” refers to partially unsaturated hydrocarbon radicals having from two to eight carbon atoms in a straight or branched chain configuration and one or more carbon-carbon triple bonds therein, including, without limitation, ethynyl, propynyl and the like. In some embodiments, C2.salkynyl includes C2_6alkynyl, C2.4alkynyl and the like. A C2.8alkynyl radical may be optionally substituted where allowed by available valences.
As used herein, the term “Ci ^alkoxy” refers to saturated hydrocarbon radicals of from one to eight carbon atoms having a straight or branched chain configuration of the formula: -O-Cj-salkyl, including, without limitation, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert-butoxy, n-pentoxy, n-hexoxy and the like. In some embodiments, Ci^alkoxy includes Ci^alkoxy, Ci_4alkoxy and the like. A Ci^alkoxy radical may be optionally substituted where allowed by available valences.
As used herein, the term “C3_i4cycloalkyl” refers to a saturated monocyclic, bicyclic or polycyclic hydrocarbon radical, including, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, ΙΗ-indanyl, indenyl, 2,3-dihydro-lH48
WO 2014/081906
PCT/US2013/07U32 indenyl, tetrahydro-naphthalenyl and the like. In some embodiments, Cs-ncycloalkyl includes Cs-scycloalkyl, Cs-scycloalkyl, C3_iocycloalkyl and the like. A C3_i4cycloalkyl radical may be optionally substituted where allowed by available valences.
As used herein, the term “aryl” refers to a monocyclic, bicyclic or polycyclic aromatic carbon atom ring structure radical, including, without limitation, phenyl, naphthyl (also referred to as naphthalenyl), anthracenyl, fluorenyl, azulenyl, phenanthrenyl and the like. An aryl radical may be optionally substituted where allowed by available valences.
As used herein, the term “heteroaryl” refers to a monocyclic, bicyclic or polycyclic aromatic carbon atom ring structure radical in which one or more carbon atom ring members have been replaced, where allowed by structural stability, with one or more heteroatoms, such as an O, S or N atom, including, without limitation, furanyl, thienyl (also referred to as thiophenyl), pyrrolyl, pyrazolyl (also referred to as lH-pyrazolyl), imidazolyl (also referred to as ΙΗ-imidazolyl), isoxazolyl (also referred to as 1,2-oxazolyl), isothiazolyl, oxazolyl, thiazolyl, triazolyl, oxadiazolyl, thiadiazolyl, tetrazolyl, pyranyl, thiopyranyl, pyridinyl (also referred to as pyridyl), pyrimidinyl, pyrazinyl, pyridazinyl, triazinyl, indolyl (also referred to as ΙΗ-indolyl), azaindolyl, indazolyl (also referred to as 2H-indazolyl), azaindazolyl, isoindolyl, indolizinyl, benzo furanyl, benzothienyl, benzimidazolyl (also referred to as 1Hbenzimidazolyl), benzothiazolyl, benzoxazolyl, imidazo[2,l-b][l,3]thiazolyl, pyrazolo[l,5ajpyridinyl, pyrazolof l,5-c]pyrimidinyl, imidazofl,2-a]pyridinyl, lH-imidazo[4,5bjpyridinyl, lH-imidazof4,5-c]pyridinyl, imidazof 1,2-a]pyrazinyl, imidazofl,2ajpyrimidinyl, 7H-purinyl, 9H-purinyl, quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, acridinyl and the like and associated homologs and regioisomers thereof. A heteroaryl radical may be optionally substituted on a carbon or nitrogen atom ring member where allowed by available valences.
As used herein, the term “heterocyclyl” refers to a saturated or partially unsaturated monocyclic, bicyclic or polycyclic carbon atom ring structure radical in which one or more carbon atom ring members have been replaced, where allowed by structural stability, with a heteroatom, such as an O, S or N atom, including, without limitation, oxiranyl, oxetanyl, azetidinyl, dihydrofuranyl, tetrahydrofuranyl, dihydrothienyl, tetrahydrothienyl, pyrrolinyl, pyrrolidinyl, dihydrop yrazolyl, pyrazolinyl, pyrazolidinyl, dihydro imidazolyl, imidazolinyl, imidazolidinyl, isoxazolinyl, isoxazolidinyl, isothiazolinyl, isothiazolidinyl, oxazolinyl,
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PCT/US2013/071132 oxazolidinyl, thiazolinyl, thiazolidinyl, triazolinyl, triazolidinyl, oxadiazolinyl, oxadiazolidinyl, thiadiazolinyl, thiadiazolidinyl, tetrazolinyl, tetrazolidinyl, 1,3-dioxolanyl, dihydro-2H-pyranyl, tetrahydro-2H-pyranyl, dihydro-pyridinyl, tetrahydro-pyridinyl, dihydro-pyrimidinyl, tetrahydro-pyrimidinyl, dihydro-pyrazinyl, tetrahydro-pyrazinyl, dihydro-pyridazinyl, tetrahydro-pyridazinyl, piperazinyl, piperidinyl, morpholinyl, thiomorpholinyl, dihydro-triazinyl, tetrahydro-triazinyl, hexahydro-triazinyl, 1,4-diazepanyl, dihydro-indolyl, indolinyl, tetrahydro-indolyl, dihydro-indazolyl, tetrahydro-indazolyl, dihydro-isoindolyl, dihydro-benzofuranyl, tetrahydro-benzofuranyl, dihydro-benzothienyl, tetrahydro-benzothienyl, dihydro-benzoimidazolyl, tetrahydro-benzoimidazolyl, dihydro-benzooxazolyl, tetrahydro-benzooxazolyl, dihydro-benzooxazinyl, tetrahydro-benzooxazinyl, benzo[l,3]dioxolyl (also referred to as 1,3-benzodioxolyl), benzo[l,4]dioxanyl (also referred to as 1,4-benzodioxanyl or 2,3-dihydro-l,4-benzodioxinyl), benzo[1,4]dioxinyl (also referred to as 1,4-benzodioxinyl), 4,5,6,7-tetrahydro-2H-indazolyl, 5,6,7,8-tetrahydroimidazo[l,2-a]pyridinyl, 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridinyl, dihydro-purinyl, tetrahydro-purinyl, dihydro-quinolinyl, tetrahydro-quinolinyl, dihydro-isoquinolinyl, tetrahydro-isoquinolinyl, dihydro-quinazolinyl, tetrahydro-quinazolinyl, dihydro-quinoxalinyl, tetrahydro-quinoxalinyl and the like and associated homologs thereof. A heterocyclyl radical may be optionally substituted on a carbon or nitrogen atom ring member where allowed by available valences.
As used herein, the term “B(OR8)2” refers to a radical of the formula: B[(-OH)(-OH)] when R8 is hydrogen; or, -B[(-OH)(-O-Ci_8alkyl)] when R8 is independently hydrogen or Ci_8alkyl; or, -B[(-O-Ci.8alkyl)(-O-Ci.8alkyl)] when R8 is Cj.8alkyl.
As used herein, the term “Cj.8alkoxy-Ci.8alkyl” refers to a radical of the formula: -Ci.8alkyl-O-Ci_8alkyl.
As used herein, the term “C].8alkoxy-Ci_8alkyl-amino” refers to a radical of the formula: -NH-Ci_8alkyl-O-Ci_8alkyl.
As used herein, the term “Ci_8alkoxy-C2_8alkenyl” refers to a radical of the formula: -C2-8alkenyl-O-Ci_8alkyl.
As used herein, the term “Cj.8alkoxy-C2-8alkynyl” refers to a radical of the formula: -C2-8alkynyl-O-Ci_8alkyl.
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As used herein, the term “C ^alkoxy-carbonyl” refers to a radical of the formula: -C(O)-O-C].8alkyl.
As used herein, the term “Cnsalkoxy-carbonyl-Ci^alkyl” refers to a radical of the formula: -Ci-8alkyl-C(O)-O-C]-8alkyl.
As used herein, the term “C].8alkoxy-carbonyl-amino” refers to a radical of the formula: -NH-C(O)-O-Ci_8alkyl.
As used herein, the term “Cnsalkoxy-carbonyl-amino-Ci-salkyl” refers to a radical of the formula: -Ci_8alkyl-NH-C(O)-O-Ci_8alkyl.
As used herein, the term “Ci-salkoxy-imino-Ci-salkyl” refers to a radical of the formula: -Ci_8alkyl(=N-O-Ci_8alkyl).
As used herein, the term “Ci.8alkyl-amino” refers to a radical of the formula: -NH-C1.8alkyl.
As used herein, the term “(Ci-8alkyl)2-amino” refers to a radical of the formula: -N(Ci_8alkyl)2.
As used herein, the term “Cp8alkyl-amino-Ci.8alkyl” refers to a radical of the formula: -Ci-salkyl-NH-Ci^alkyl.
As used herein, the term “(Ci.8alkyl)2-amino-Ci.8alkyl” refers to a radical of the formula: -Ci.8alkyl-N(Ci.8alkyl)2.
As used herein, the term “Ci-salkyl-amino-Ci_8alkyl-amino” refers to a radical of the formula:-NH-Ci.8alkyl-NH-Ci_8alkyl.
As used herein, the term “(Ci-8alkyl)2-amino-Ci-8alkyl-amino” refers to a radical of the formula: -NH-Ci.8alkyl-N(Ci_8alkyl)2.
As used herein, the term “Ci-salkyl-amino-carbonyl” refers to a radical of the formula: -C(O)-NH-C|.8alkyl.
As used herein, the term “(Ci-8alkyl)2-amino-carbonyl” refers to a radical of the formula: -C(O)-N(Ci_8alkyl)2.
As used herein, the term “Cj.salkyl-amino-carbonyl-amino” refers to a radical of the formula: -NH-C(O)-NH-Ci_8alkyl.
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As used herein, the term “(Ci-8alkyl)2-amino-carbonyl-amino” refers to a radical of the formula: -NH-C(O)-N(Ci.8alkyl)2.
As used herein, the term “Ci-salkyl-amino-sulfonyl” refers to a radical of the formula: -SO2-NH-Ci_8alkyl.
As used herein, the term “(Ci-salkyl^-amino-sulfonyl” refers to a radical of the formula: -SO2-N(Cj.8alkyl)2.
As used herein, the term “Ci_8alkyl-amino-sulfonyl-amino” refers to a radical of the formula: -NH-SO2-NH-Ci.8alkyl.
As used herein, the term “(Ci_8alkyl)2-amino-sulfonyl-amino” refers to a radical of the formula: -NH-SC>2-N(Ci.8alkyl)2.
As used herein, the term “Ci.8alkyl-carbonyl” refers to a radical of the formula: -C(O)-Ci.8alkyl.
As used herein, the term “Ci_8alkyl-carbonyl-amino” refers to a radical of the formula: -NH-C(O)-Ci_8alkyl.
As used herein, the term “Ci.8alkyl-carbonyl-amino-Ci.8alkyl” refers to a radical of the formula: -Ci_8alkyl-NH-C(O)-Ci.8alkyl.
As used herein, the term “Ci.8alkyl-carbonyl-oxy” refers to a radical of the formula: -O-C(O)-Ci_8alkyl.
As used herein, the term “Ci.8alkyl-carbonyl-oxy-Ci.8alkyl” refers to a radical of the formula: -C].8alkyl-O-C(O)-Ci.8alkyl.
As used herein, the term “C].8alkyl-sulfonyl” refers to a radical of the formula: -SO2-Ci_8alkyl.
As used herein, the term “Ci_8alkyl-thio” refers to a radical of the formula: -S-C].8alkyl.
As used herein, the term “amino” refers to a radical of the formula: -NH2.
As used herein, the term “amino-C[_8alkyl” refers to a radical of the formula: -Ci_8alkyl-NH2.
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As used herein, the term “amino-Ci.galkyl-amino” refers to a radical of the formula: -Nll-C|_xalkyl-Nll2.
As used herein, the term “amino-carbonyl” refers to a radical of the formula: -C(O)-NH2.
As used herein, the term “amino-carbonyl-amino” refers to a radical of the formula: -NH-C(O)-NH2.
As used herein, the term “amino-sulfonyl” refers to a radical of the formula: -SO2-NH2.
As used herein, the term “amino-sulfonyl-amino” refers to a radical of the formula: -NH-SO2-NH2.
As used herein, the term “aryl-Ci^alkyl” refers to a radical of the formula: -Cpsalkyl-aryl.
As used herein, the term “aryl-Ci^alkyl-amino” refers to a radical of the formula: -NH-Ci-salkyl-aryl.
As used herein, the term “aryl-amino” refers to a radical of the formula: -NH-aryl.
As used herein, the term “carboxyl” refers to a radical of the formula: -COOH, -C(O)OH or -CO2H.
As used herein, the term “formyl” refers to a radical of the formula: -C(O)-H.
As used herein, the term “formyl-oxyl” refers to a radical of the formula: -O-C(O)-H.
As used herein, the terms “halo” or “halogen” refer to a halogen atom radical, including fluoro, chloro, bromo and iodo.
As used herein, the tenia “halo-C ^alkoxy” refers to a radical of the fonnula: -O-C|_xalkyl-halo, wherein Ci-galkyl may be partially or completely substituted where allowed by available valences with one or more halogen atoms. In some embodiments, halo-Cj-salkoxy includes halo-Ci_6alkoxy, halo-Ci_4alkoxy and the like.
As used herein, the term “halo-Ci-galkoxy-carbonyl” refers to a radical of the foimula: -C(O)-O-C]_8alkyl-halo.
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As used herein, the term “halo-Ci_8alkyl” refers to a radical of the formula: -Ci_8alkyl-halo, wherein Cj.«alkyl may be partially or completely substituted where allowed by available valences with one or more halogen atoms. In some embodiments, halo-Cj-salkyl includes halo-Ci^alkyl, halo-Ci.4alkyl and the like.
As used herein, the term “halo-Ci.8alkyl-carbonyl” refers to a radical of the formula: -C(O)-C].8alkyl-halo.
As used herein, the term “halo-Ci-salkyl-sulfonyl” refers to a radical of the formula: -SO2-Ci_8alkyl-halo.
As used herein, the term “halo-C«8alkyl-thio” refers to a radical of the formula: -S-Ci_8alkyl-halo.
As used herein, the term “heteroaryl-Ci_8alkyl” refers to a radical of the formula: -Ci_8alkyl-heteroaryl.
As used herein, the term “hydroxyl-Ci_8alkoxy” refers to a radical of the formula: -O-Ci_8alkyl-OH, wherein Ci_8alkyl may be partially or completely substituted where allowed by available valences with one or more hydroxyl radicals.
As used herein, the term “hydroxyl-Ci_8alkyl” refers to a radical of the formula: -C«8alkyl-OH, wherein Ci_8alkyl may be partially or completely substituted where allowed by available valences with one or more hydroxyl radicals.
As used herein, the term “hydroxyl-amino” refers to a radical of the formula:-NH-OH.
As used herein, the term “hydroxyl-Ci_8alkyl-amino” refers to a radical of the formula: -NH-Ci_8alkyl-OH.
As used herein, the term “hydroxyl-Ci_8alkyl-amino-Ci_8alkyl” refers to a radical of the formula: -Ci_8alkyl-NH-C]-8alkyl-OH.
As used herein, the term “hydroxyl-Ci.8alkyl-amino-Ci.8alkyl-ammo” refers to a radical of the formula: -NH-Ci_8alkyl-NH-C].8alkyl-OH.
As used herein, the term “hydroxyl-imino-Cj.8alkyl” refers to a radical of the formula: -Cj.8alkyl(=N-OH).
As used herein, the term “imino” refers to a radical of the formula: =NH.
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As used herein, the term “imino-Ci-salkyl” refers to a radical of the formula: -C]_8alkyl(=NH).
Figure AU2013348009C1_D0107
As used herein, the term “N-oxide” refers to a moiety of the formula: O .
As used herein, the term “oxo” refers to a moiety of the formula:
O
Figure AU2013348009C1_D0108
As used herein, the term “P(O)(R7)2-amino” refers to a radical of the formulae: -NH-P(O)(-O-Ci_8alkyl)(OH) when R7 is independently hydroxyl and (Ci.8alkoxy)n, where n is 1; or, -NH-P(O)(OH)2 when R7 is hydroxyl;
or, -NH-P(O)(-O-Ci_8alkyl)2 when R7 is (Ci_8alkoxy)n, where n is 1.
As used herein, the term “substituent” means positional variables on the atoms of a core molecule that are attached at a designated atom position, replacing one or more hydrogen atoms on the designated atom, provided that the atom of attachment does not exceed the available valence or shared valence, such that the substitution results in a stable compound. Accordingly, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds. Any carbon atom as well as heteroatom with a valence level that appears to be unsatisfied as described or shown herein is assumed to have a sufficient number of hydrogen atom(s) to satisfy the valences described or shown.
As used herein, the term “and the like,” with reference to the definitions of chemical terms provided herein, means that variations in chemical structures that could be expected by one skilled in the art include, without limitation, isomers (including chain, branching or positional structural isomers), hydration of ring systems (including saturation or partial unsaturation of monocyclic, bicyclic or polycyclic ring structures) and all other variations where allowed by available valences which result in a stable compound.
For the purposes of this description, where one or more substituent variables for a compound of Formula (I) encompass functionalities incorporated into a compound of Formula (I), each functionality appearing at any location within the disclosed compound may be independently selected, and as appropriate, independently and/or optionally substituted.
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As used herein, the terms “independently selected,” or “each selected” refer to functional variables in a substituent list that may be attached more than once on the structure of a core molecule, where the pattern of substitution at each occurrence is independent of the pattern at any other occurrence. Further, the use of a generic substituent variable on a core structure for a compound described herein is understood to include the replacement of the generic substituent with specie substituents that are included within the particular genus, e.g., aryl may be replaced with phenyl or naphthalenyl and the like, such that the resulting compound is to be included within the scope of the compounds described herein.
As used herein, the term “optionally substituted” means that the specified substituent variables, groups, radicals or moieties represent the scope of the genus and may be independently chosen as needed to replace one or more hydrogen atoms on the designated atom of attachment of a core molecule.
As used herein, the terms “stable compound’ or “stable structure” mean a compound that is sufficiently robust to be isolated to a useful degree of purity from a reaction mixture and formulations thereof into an efficacious therapeutic agent.
Compound names used herein were obtained using the ACD Labs Index Name software provided by ACD Labs and/or ChemDraw Ultra software provided by CambridgeSoft. When the compound name disclosed herein conflicts with the structure depicted, the structure shown will supercede the use of the name to define the compound intended.
Compound Forms
As used herein, the terms a “compound of Formula (la),” “a compound of Formula (II),” “compound of Formula (Ila),” “compound of Formula (III),” “compound of Formula (Illa),” “compound of Formula (IV)” or “compound of Formula (IVa)” refer to subgenera of the compound of Formula (I) or a form thereof, as defined herein. Rather than repeat the various subgenera of the compound of Formula (I), in certain embodiments, the term “compound(s) of Formula (I) or a form thereof’ is used inclusively to refer to compound(s) of Formula (la) or a form thereof, compound(s) of Formula (II) or a form thereof, compound(s) of Formula (Ila) or a form thereof, compound(s) of Formula (III) or a form thereof, compound(s) of Formula (Illa) or a form thereof, compound(s) of Formula (IV) or a
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PCT/US2013/071132 form thereof or compound(s) of Formula (IVa) or a form thereof, either separately or together. Thus, embodiments and references to “a compound of Formula (1)” are intended to be inclusive of compounds of Formula (la), compounds of Formula (II), compounds of Formula (Ila), compounds of Formula (III), compounds of Formula (Illa), compounds of Formula (IV) and compounds of Formula (IVa).
As used herein, the term “form” means a compound of Formula (I) selected from a free acid, free base, salt, ester, hydrate, solvate, chelate, clathrate, polymorph, isotopologue, stereoisomer, racemate, enantiomer, diastereomer, or tautomer thereof.
In certain embodiments described herein, the form of the compound of Formula (I) is selected from a salt, isotopologue, stereoisomer, racemate, enantiomer, diastereomer or tautomer thereof.
In certain embodiments described herein, the form of the compound of Formula (I) is selected from a free acid, isotopologue, stereoisomer, racemate, enantiomer, diastereomer or tautomer thereof.
In certain embodiments described herein, the form of the compound of Formula (I) is selected from a free base, isotopologue, stereoisomer, racemate, enantiomer, diastereomer or tautomer thereof.
In certain embodiments described herein, the form of the compound of Formula (I) is a free acid, free base or salt thereof.
In certain embodiments described herein, the form of the compound of Formula (I) is an isotopologue thereof.
In certain embodiments described herein, the form of the compound of Formula (I) is a stereoisomer, racemate, enantiomer or diastereomer thereof.
In certain embodiments described herein, the form of the compound of Formula (I) is a tautomer thereof.
In certain embodiments described herein, the form of the compound of Formula (I) is a pharmaceutically acceptable form.
In certain embodiments described herein, the compound of Formula (I) or a form thereof is isolated for use.
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As used herein, the term “isolated” means the physical state of a compound of Formula (I) or a form thereof after being isolated and/or separated and/or purified from a synthetic process (e.g., from a reaction mixture) or natural source or combination thereof according to an isolation, separation or purification process or processes described herein or which are well known to the skilled artisan (e.g., chromatography, recrystallization and the like) in sufficient purity to be characterizable by standard analytical techniques described herein or well known to the skilled artisan.
As used herein, the term “protected” means that a functional group on a compound of Formula (I) or a form thereof is in a form modified to preclude undesired side reactions of the functional group when the compound is subjected to a reaction. Suitable protecting groups will be recognized by those with ordinary skill in the art as well as by reference to standard textbooks such as, for example, T. W. Greene et al, Protective Groups in Organic Synthesis (2007), Wiley, New York.
Prodrugs and solvates of the compounds of Formula (I) or a form thereof described herein are also contemplated.
As used herein, the term “prodrug” means that a functional group on a compound of Formula (I) is in a form (e.g., acting as an active or inactive drug precursor) that is transformed in vivo to yield an active or more active compound of Formula (I) or a form thereof. The transformation may occur by various mechanisms (e.g., by metabolic and/or non-metabolic chemical processes), such as, for example, by hydrolysis and/or metabolism in blood, liver and/or other organs and tissues. A discussion of the use of prodrugs is provided by V.J. Stella, et. al., “Biotechnology: Pharmaceutical Aspects, Prodrugs: Challenges and Rewards,” American Association of Pharmaceutical Scientists and Springer Press, 2007.
In one example, when a compound of Formula (I) or a form thereof contains a carboxylic acid functional group, a prodrug can comprise an ester formed by the replacement of the hydrogen atom of the acid group with a functional group such as alkyl and the like. In another example, when a compound of Formula (I) or a form thereof contains an alcohol functional group, a prodrug can be formed by the replacement of the hydrogen atom of the alcohol group with a functional group such as alkyl or carbonyloxy and the like. In another example, when a compound of Formula (I) or a form thereof contains an amine functional
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PCT/US2013/071132 group, a prodrug can be formed by the replacement of one or more amine hydrogen atoms with a functional group such as alkyl or substituted carbonyl.
Pharmaceutically acceptable prodrugs of compounds of Formula (I) or a form thereof include those compounds substituted with one or more of the following groups: carboxylic acid esters, sulfonate esters, amino acid esters, phosphonate esters (e.g., a phosphoramidic acid used to derive a phosphoramidic acid) and mono-, di- or triphosphate esters further substituted with alkyl, where appropriate. As described herein, it is understood by a person of ordinary skill in the art that one or more of such substituents may be used to provide a compound of Formula (I) or a form thereof as a prodrug.
The compounds of Formula (I) or a form thereof can form salts, which are intended to be included within the scope of this description. Reference to a compound of Formula (I) or a form thereof herein is understood to include reference to salts thereof, unless otherwise indicated. The term salt(s), as employed herein, denotes acidic salts formed with inorganic and/or organic acids, as well as basic salts formed with inorganic and/or organic bases. In addition, when a compound of Formula (I) or a form thereof contains both a basic moiety, such as, but not limited to a pyridine or imidazole, and an acidic moiety, such as, but not limited to a carboxylic acid, zwitterions (inner salts) may be formed and are included within the term salt(s) as used herein.
The term pharmaceutically acceptable salt(s), as used herein, means those salts of compounds of Formula (I) or a form thereof described herein that are safe and effective (i.e., non-toxic, physiologically acceptable) for use in mammals and that possess biological activity, although other salts are also useful. Salts of the compounds of the Formula (I) may be formed, for example, by reacting a compound of Formula (I) with an amount of acid or base, such as an equivalent amount, in a medium such as one in which the salt precipitates or in an aqueous medium followed by lyophilization.
Pharmaceutically acceptable salts include one or more salts of acidic or basic groups present in compounds of Formula (I) or a form thereof described herein. Embodiments of acid addition salts include, and are not limited to, acetate, acid phosphate, ascorbate, benzoate, benzenesulfonate, bisulfate, bitartrate, borate, butyrate, chloride, citrate, camphorate, camphorsulfonate, ethanesulfonate, formate, fumarate, gentisinate, gluconate, glucaronate, glutamate, hydrobromide, hydrochloride, dihydrochloride, hydroiodide,
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PCT/US2013/071132 isonicotinate, lactate, maleate, methanesulfonate, naphthalenesulfonate, nitrate, oxalate, pamoate, pantothenate, phosphate, propionate, saccharate, salicylate, succinate, sulfate, tartrate, thiocyanate, toluenesulfonate (also known as tosylate), trifluoroacetate, trifluoroacetic acid salt and the like. One or more embodiments of acid addition salts include chloride, hydrochloride, dihydrochloride, trihydrochloride, hydrobromide, acetate, diacetate, methanesulfonate, sulfate, trifluoro acetate, trifluoroacetic acid salt and the like. More particular embodiments include a chloride, hydrochloride, dihydrochloride, hydrobromide, methanesulfonate, sulfate, trifluoroacetate, trifluoroacetic acid salt and the like.
In certain embodiments of the compounds of Formula (I) or a form thereof described herein, the compound is isolated as a salt form, wherein the compound is conjugated with the salt in a ratio represented as, in a non-limiting example, “compound’.salt (A:B),” wherein “A” and “B” represent the equivalents of compound to salt in the isolated form.
Additionally, acids which are considered suitable for the formation of pharmaceutically useful salts from basic pharmaceutical compounds are discussed, for example, by P. Stahl et al, Camille G. (eds.) Handbook of Pharmaceutical Salts. Properties, Selection and Use. (2002) Zurich: Wiley-VCH; S. Berge et al, Journal of Pharmaceutical Sciences (1977) 66(1) 1-19; P. Gould, International J. of Pharmaceutics (1986) 33, 201-217; Anderson et al, The Practice of Medicinal Chemistry (1996), Academic Press, New York; and in The Orange Book (Food & Drug Administration, Washington, D.C. on their website). These disclosures are incorporated herein by reference thereto.
Suitable basic salts include, but are not limited to, aluminum, ammonium, calcium, lithium, magnesium, potassium, sodium, zinc, and diethanolamine salts. Certain compounds of Formula (I) or a form thereof described herein can also form pharmaceutically acceptable salts with organic bases (for example, organic amines) such as, but not limited to, dicyclohexylamines, tert-butyl amines and the like, and with various amino acids such as, but not limited to, arginine, lysine and the like. Basic nitro gen-containing groups may be quartemized with agents such as lower alkyl halides (e.g., methyl, ethyl, and butyl chlorides, bromides and iodides), dialkyl sulfates (e.g., dimethyl, diethyl, and dibutyl sulfates), long chain halides (e.g., decyl, lauryl, and stearyl chlorides, bromides and iodides), aralkyl halides (e.g., benzyl and phenethyl bromides), and others.
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All such acid salts and base salts are intended to be included within the scope of pharmaceutically acceptable salts as described herein. In addition, all such acid and base salts are considered equivalent to the free forms of the corresponding compounds for purposes of this description.
Compounds of Formula (I), and forms thereof, may further exist in a tautomeric form. All such tautomeric forms are contemplated and intended to be included within the scope of the compounds of Formula (I) or a form thereof as described herein.
The compounds of Formula (I) or a form thereof may contain asymmetric or chiral centers, and, therefore, may exist in different stereoisomeric forms. The present description is intended to include all stereoisomeric forms of the compounds of Formula (!) as well as mixtures thereof, including racemic mixtures.
The compounds of Formula (I) or a form thereof described herein may include one or more chiral centers, and as such may exist as racemic mixtures (R/S) or as substantially pure enantiomers and diastereomers. The compounds may also exist as substantially pure (7?) or (5) enantiomers (when one chiral center is present). In one embodiment, the compounds of Formula (I) or a form thereof described herein are (5) isomers and may exist as enantiomerically pure compositions substantially comprising only the (5) isomer. In another embodiment, the compounds of Formula (I) or a form thereof described herein are (R) isomers and may exist as enantiomerically pure compositions substantially comprising only the (/?) isomer. As one of skill in the art will recognize, when more than one chiral center is present, the compounds of Formula (I) or a form thereof described herein may also exist as a (R,R), (R,S), (S,R) or (S,S) isomer, as defined by IUPACNomenclature Recommendations.
As used herein, the term “substantially pure” refers to compounds of Formula (I) or a form thereof consisting substantially of a single isomer in an amount greater than or equal to 90%, in an amount greater than or equal to 92%, in an amount greater than or equal to 95%, in an amount greater than or equal to 98%, in an amount greater than or equal to 99%, or in an amount equal to 100% of the single isomer.
In one aspect of the description, a compound of Formula (I) or a form thereof is a substantially pure (5) enantiomer present in an amount greater than or equal to 90%, in an amount greater than or equal to 92%, in an amount greater than or equal to 95%, in an
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PCT/US2013/071132 amount greater than or equal to 98%, in an amount greater than or equal to 99%, or in an amount equal to 100%.
In one aspect of the description, a compound of Formula (I) or a form thereof is a substantially pure (/?) enantiomer present in an amount greater than or equal to 90%, in an amount greater than or equal to 92%, in an amount greater than or equal to 95%, in an amount greater than or equal to 98%, in an amount greater than or equal to 99%, or in an amount equal to 100%.
As used herein, the term “racemate” refers to any mixture of isometric forms that are not “enantiomerically pure”, including mixtures such as, without limitation, in a ratio of about 50/50, about 60/40, about 70/30, or about 80/20, about 85/15 or about 90/10.
In addition, the compounds of Formula (I) or a form thereof described herein embrace all geometric and positional isomers. For example, if a compound of Formula (I) or a form thereof incorporates a double bond or a fused ring, both the cis- and trans-forms, as well as mixtures thereof, are embraced within the scope of the compounds of Formula (I) or a form thereof described herein.
Diastereomeric mixtures can be separated into their individual diastereomers on the basis of their physical chemical differences by methods well known to those skilled in the art, such as, for example, by chromatography and/or fractional crystallization. Enantiomers can be separated by use of a chiral HPLC column or other chromatographic methods known to those skilled in the art.
Enantiomers can also be separated by converting the enantiomeric mixture into a diastereomeric mixture by reaction with an appropriate optically active compound (e.g., chiral auxiliary such as a chiral alcohol or Mosher’s acid chloride), separating the diastereomers and converting (e.g., hydrolyzing) the individual diastereomers to the corresponding pure enantiomers.
All stereoisomers (for example, geometric isomers, optical isomers and the like) of the present compounds of Formula (I) or a form thereof (including salts, solvates, esters and prodrugs and transformed prodrugs thereof), which may exist due to asymmetric carbons on various substituents, including enantiomeric forms (which may exist even in the absence of asymmetric carbons), rotameric forms, atropisomers, diastereomeric and regioisomeric forms, are contemplated within the scope of the description herein. Individual stereoisomers of the 62
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PCT/US2013/071132 compounds of Formula (I) or a form thereof described herein may, for example, be substantially free of other isomers, or may be present in a racemic mixture, as described supra.
The use of the terms salt, solvate, “ester,” prodrug and the like, is intended to apply equally to the salt, solvate, ester and prodrug of enantiomers, stereoisomers, rotamers, tautomers, positional isomers, racemates, isotopologues or prodrugs of the instant compounds.
The term isotopologue refers to isotopically-enriched compounds of Formula (I) or a form thereof which are identical to those recited herein, but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature. Examples of isotopes that can be incorporated into compounds of Formula (I) or a form thereof described herein include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, fluorine and chlorine, such as Η2, H3, C13, C14, N15, Ο18, Ο17, P31, P32, S35, F18, Cl35 and Cl36, respectively, each of which is also within the scope of this description.
Certain isotopically-enriched forms of compounds of Formula (I) or a form thereof described herein (e.g., those labeled with H3 and C14) are useful in compound and/or substrate tissue distribution assays. Tritiated (i.e., H3) and carbon-14 (i.e., C14) isotopes are particularly preferred for their ease of preparation and detectability. Further, substitution with isotopes such as deuterium (i.e., deuterium enriched) may afford certain therapeutic advantages resulting from greater metabolic stability (e.g., increased in vivo half-life), increased solubility, reduced dosage requirements (e.g., increased bioavailability)) or reduced toxicity (e.g., reduced inhibition of metabolic enzymes) and hence may be preferred in some circumstances.
One or more compounds of Formula (1) or a form thereof described herein may exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like, and the description herein is intended to embrace both solvated and unsolvated forms.
As used herein, the term “solvate” means a physical association of a compound of Formula (I) or a form thereof described herein with one or more solvent molecules. This physical association involves varying degrees of ionic and covalent bonding, including
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PCT/US2013/071132 hydrogen bonding. In certain instances the solvate will be capable of isolation, for example when one or more solvent molecules are incorporated in the crystal lattice of the crystalline solid. As used herein, “solvate” encompasses both solution-phase and isolatable solvates. Non-limiting examples of suitable solvates include ethanolates, methanolates, and the like.
One or more compounds of Formula (I) or a form thereof described herein may optionally be converted to a solvate. Preparation of solvates is generally known. A typical, non-limiting process involves dissolving a compound of Formula (I) or a form thereof in a desired amount of the desired solvent (organic or water or mixtures thereof) at a higher than ambient temperature, and cooling the solution at a rate sufficient to form crystals which are then isolated by standard methods. Analytical techniques such as, for example infrared spectroscopy, show the presence of the solvent (or water) in the crystals as a solvate (or hydrate).
As used herein, the term “hydrate” means a solvate wherein the solvent molecule is water.
Polymorphic crystalline and amorphous forms of the compounds of Formula (I) or a form thereof, and of the salts, solvates, esters and prodrugs of the compounds of Formula (I) or a form thereof, are further intended to be included in the scope of the compounds of Formula (I) or a form thereof described herein.
Compound Uses
The Bmi-1 oncogene was first identified as part of a key insertion/activation region of the Moloney murine leukemia virus in the early 1990’s (7-6). Bmi-1 is a member of the Polycomb group (PcG) of transcriptional repressors and was identified as a necessary regulator of hematopoietic stem cell (HSC) self-renewal (76, 77). Park found that Bmi-1 is highly expressed in purified mouse and human HSCs and that the absence of Bmi-1, as demonstrated by Bmi-1 knockout mice, results in the progressive loss of all hematopoietic lineages (76). Furthermore, the transplantation of Bmi-Γ1' day 14.5 fetal liver cells into lethally irradiated normal mice, demonstrated that the cells were unable to reconstitute myeloid cells, B cells, and T cells because Bmi-T1' HSCs were unable to renew (76).
In addition to the role of Bmi-1 in HSC self renewal, it was found that Bmi-1 transgene expression induced lymphoma in mice (2). Bmi-1 was also found to be
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PCT/US2013/071132 overexpressed in many tumor types, including acute myeloid leukemia, medulloblastoma, neuroblastoma, colorectal cancer, lung cancer, and prostate cancer, and was found to increase with malignancy (34, 78, 61, 79, 80, 65, 43). Loss of Bmi-1 in various human cancer cell lines via Bmi-1 specific RNA interference (RNAi) was shown to lead to acute cell death and growth inhibition, whereas loss of Bmi-1 in various normal cell lines was shown to lead to only moderate growth inhibition and not significant cell death (69). Thus, Bmi-1 is necessary for the survival of cancer cells but has minimal effect on the survival of normal cells.
Bmi-1 has been subsequently shown to act as an oncogene experimentally and has proven particularly potent in conjunction with c-myc to initiate lymphoma in mice (7, 8). The role of Bmi-1 in lymphomagenesis has been attributed partially to transcriptional repression of the INK4a locus (containing both the pl6INK4A and pl4ARF genes) leading to maintenance of cancer and tumor cell proliferation and prevention of differentiation (7,9). Loss of expression of the INK4a locus due to promoter silencing has been extensively studied and is both important for the progression and prognosis of many types of hematologic cancers (10, 11). The INK4a locus is occasionally lost by deletion in leukemia and lymphoma (12, 13).
However, Bmi-1 has been shown to play a role in tumorigenesis in models lacking the INK4a locus, indicating that other loci important in cancer are regulated by this protein (14). Experimental results have demonstrated further that loss of Bmi-1 induces growth arrest and senescence in fibrosarcoma cells known to lack INK4a (15). There is also evidence that Bmi-1 is important for the hedgehog (Hh) pathway in breast cancer. Activation of Hh signaling increases Bmi-1 expression, while down-regulation of Bmi-1 (via siRNA) abrogates the effects of Hh signaling on mammosphere formation in vitro and inhibits ductal/alveolar development in mice (16). Recent work has demonstrated the role of Bmi-1 in the regulation of Hox gene expression. Knockdown of Bmi-1 caused a global and loci-specific loss of H2A ubiquitination, upregulation of the HoxC5 gene, and inhibition of the growth of HeLa cells (17). Another study demonstrated that E2F6 and Bmi-1 cooperate in the regulation of Hox gene expression (particularly Hox C10 and B9), and consequently affect axial skeleton development, but not in the repression of the Ink4a-Arf locus. These findings underscore the significance of the E2F6-Bmi-1 interaction and suggest that the Hox and Ink4a-Arf loci are regulated by somewhat different Bmi-1-dependent mechanisms (18). Current research
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PCT/US2013/071132 suggests that Bmi-1 has different roles dependent upon cell types and/or developmental stages. Other genes regulated by Bmi-1 remain to be identified.
Bmi-1 is found to be highly expressed in malignancies, such as diffuse large B cell lymphomas (DLBCL), B cell non-Hodgkin’s lymphoma, Hodgkin’s lymphoma, acute myeloid leukemia, colorectal carcinoma, liver carcinoma, non-small cell lung cancer, breast carcinoma and medulloblastoma. The study of Bmi-1 knockout mice has revealed that Bmi-1 is required for the self-renewal of both leukemic and normal hematopoietic stem cells.
Additionally, evidence exists linking Bmi-1 levels to blood tumor types, particularly Burkitt’s lymphoma, mantle cell lymphoma, Hodgkin’s lymphoma (21-23), non-Hodgkin’s lymphoma, some T cell lymphomas (2, 24-31), acute myeloid leukemia and T-ALL (32-35). Raaphorst et al observed that, in Hodgkin’s lymphoma, Reed-Sternberg cells (HRS) coexpress Bmi-1, EZH2, and Mib-l/Ki-67. Because HRS cells are thought to originate from germinal center lymphocytes that express Bmi-1, such lymphocytes should lose the ability to express Bmi-1 (and gain the ability to express EZH2) as they differentiate. These observations suggest that Hodgkin’s lymphoma is associated with aberrant co-expression of Bmi-1 and EZH2 in these cells (22). An assessment of acute myeloid leukemia stem cell populations by van Gosliga et al (36) showed that CD34+/CD38 cells capable of forming leukemic-cobblestone colonies on a bone marrow substrate through at least two rounds of expansion represented an extreme minority of the cell population. Further analysis showed that this cell population expresses high levels of Bmi-1 mRNA and can establish an aggressive leukemia in mice, while those cells that have lower levels of Bmi-1 mRNA cannot (36). Such studies implicate Bmi-1 in tumor growth and cell survival and suggest a central function in tumor initiation and maintenance of cancer and tumor stem cells.
The levels of Bmi-1 have been shown to have prognostic relevance in a number of tumor types. An example of this is found in acute myeloid leukemia based on results from a study assessing the prognostic value of high Bmi-1 levels in 64 patients (32). On the basis of the median value of Bmi-1 (54.58%), patients were divided into two groups and monitored for survival. Patients with lower Bmi-1 positivity (<55%, n=33) had significantly longer overall survival (P=0.0001), relapse-free survival (P=0.0072) and remission duration (7+=0.0065) when compared to the patients with higher levels of Bmi-1 (>55%, n=31, respectively), regardless of age group (32). Similarly, Van Galen et al (37) have shown that
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Bmi-1 levels are highly prognostic in diffuse large B cell lymphomas (DLBCL) (37). Neoplastic cells in DLBCL cases originate from germinal centre B (GCB) cells or their descendents(3<S). Recent microarray analyses have shown that some DLBCL phenotypically resemble non-neoplastic GCB cells, while some show an expression profile similar to that of activated B cells (ABC) (39).
Furthermore, patients with a GCB-like phenotype have a considerably better prognosis than those with an ABC-like phenotype (40). Bmi-1 was identified as one of the genes that distinguish the ABC-like DLBCL (39),(41). Other groups have linked elevated Bmi-1 levels with poor prognosis in mantle cell lymphoma (MCL), non-Hodgkin’s lymphoma and other leukemias (22, 26, 27, 29, 42-44), as well as many other tumour types including neuroblastoma, glioblastoma, hepatocellular carcinoma, and breast, colorectal, prostate, lung, gastric and salivary gland cancers (45-57). The loss of expression from the INK4A locus has also been shown to have prognostic value (12, 13). Taken together, these data strongly implicate Bmi-1 in cancer and suggest that inhibiting uncontrolled cell proliferation by inhibiting Bmi-1 function and reducing the level of Bmi-1 in a cancer cell, tumor cell, cancer stem cell or tumor stem cell will have a beneficial therapeutic effect in patients with multiple cancer types, particularly in those afflicted with hematological cancers.
For example, MCL is a rare, aggressive and incurable B cell non-Hodgkin’s lymphoma that is refractory (i.e., resistant to conventional chemotherapy) and is associated with a poor prognosis. MCL is characterized by the t(l 1 ;14)(ql3;q32) translocation, resulting in amplification and overexpression of the polycomb group gene Bmi-1, which normally functions for self-renewal of hematopoietic stem cells but has the capacity to induce tumors when overexpressed.
Multiple myeloma is another fatal B-cell malignancy characterized by the accumulation of abnormal plasma cells in the bone marrow. Standard therapy for multiple myeloma is similar to the course for MCL and normally consists of combination chemotherapy that often results in a 60-70% response rate. However, most patients will eventually relapse, leaving patients with limited therapeutic options. Recent gene expression profiling of multiple myeloma cells revealed elevated expression of Bmi-1 compared to that in normal plasma cells, as confirmed by immunoblotting.
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Bmi-1 has been shown to be regulated transcriptionally by a number of factors including SALL4, FoxMl, c-Myc, E2F-1 and Mell8. Bmi-1 and SALL4 are putative oncogenes that modulate stem cell pluripotency and play a role in leukemigenesis (also referred to as leukemogenesis). Murine Sall4 also has been shown to play an essential role in maintaining the properties of ES (embryonic stem) cells and governing the fate of the primitive inner cell mass. Yang et al demonstrated that transcription from the Bmi-1 promoter is markedly activated by SALL4 in a dose-dependent manner (35). The Forkhead box transcription factor FoxMl is expressed in proliferating cells and has been shown to upregulate the levels of Bmi-1 in transformed NIH 3T3 cells in response to oxidative stress through c-myc activation (58). The Bmi-1 homologue, Mell 8, acts as a potent repressor on the expression of Bmi-1. The Bmi-1 promoter region contains a functional E-box through which c-Myc and Mel-18 can regulate Bmi-1 expression. Since Mel 18 downregulates c-Myc expression and Bmi-1 is a c-Myc target, these data suggest that Mell 8 regulates expression of Bmi-1 via repression of c-Myc during cellular senescence and, thus, link c-Myc and polycomb function (59). Similarly, a recent report suggests that E2F-1 may also regulate the levels of Bmi-1 in neuroblastoma (60). The Bmi-1 promoter contains aputative E2F binding site required for the activation of a Bmi-1 promoter-dependent reporter construct by E2F-1. Neither post-transcriptional nor post-translational control of Bmi-1 production has been reported.
Without being limited by theory, the compounds of Formula (I) or a form thereof described herein activate the apoptotic pathway as determined by annexin-V expression, as well as cleavage of poly (ADP-ribose) polymerase (PARP) and caspase-9 and caspase-7. Cell cycle analyses of cells treated with these compounds of Formula (I) or a form thereof have further demonstrated a block at the G2/M phase followed by the development of polyploidy. These findings suggest that Bmi-1 may also play a role in DNA repair and/or regulation of mitosis. The compounds of Formula (I) or a form thereof described herein are useful inhibitors of Bmi-1 function and cause a reduction in the level of Bmi-1 protein and are thus potential therapeutics for any cancer cell, tumor cell, cancer stem cell or tumor stem cell that overexpresses Bmi-1. Additionally, the compounds of Formula (I) or a form thereof described herein inhibit the function of Bmi-1 and reduce Bmi-1 levels in cancer stem cell and tumor stem cell environments and are thus useful in targeting cancer cell populations that have been shown to be resistant to current therapies (e.g., such as those using large and small
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PCT/US2013/071132 molecule chemotherapeutic agents and radiation therapies, as well as targeted therapies that primarily function by indiscriminately damaging mitotic cells).
As used herein, the italicized form of “Rmz-7,” unless otherwise specified or clear from the context of the specification, refers to the Bmi-1 gene. The nonitalicized form of “Bmi-1,” the capitalized form of “BMI-1” or the term “Bmi-1 protein,” unless otherwise specified or clear from the context of the specification, collectively refer to Bmi-1 protein.
As used herein, the term “Bmi-1 inhibitor” or the phrase (or variations thereof) “inhibit Bmi-1 function and reduce the level of Bmi-1” refer to post-translational inhibition of the function of Bmi-1 protein and subsequent degradation, resulting in decreased levels of Bmi-1 protein present in a tumor environment including, but not limited to, in vitro and in vivo environments comprising cancer stem cells or tumor stem cells or cancer stem cells and tumor stem cells.
In accordance with the present description, compounds of Formula (I) or a form thereof that inhibit Bmi-1 function and reduce the level of Bmi-1 also inhibit proliferation of tumor cells in vitro and in vivo and enhance sensitivity of intrinsically resistant populations (e.g., either “cancer stem cells,” “tumor stem cells” or both) to chemotherapeutics. Elevated expression of human Bmi-1 has been reported in multiple cancer samples and cancer cell lines (2, 42, 51, 56, 61-68). Applicants have identified compounds of Formula (I) or a form thereof that inhibit Bmi-1 function and reduce the level of Bmi-1 in vitro and in vivo, with concurrent inhibition of tumor cell growth and xenograft growth in vivo.
One embodiment described herein is directed to a method of inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising contacting a cell having elevated Bmi-1 levels from the subject with an amount of a compound of Formula (I) or a form thereof, wherein the cell is selected from a cancer cell, tumor cell, cancer stem cell or tumor stem cell, determining an effective amount of the compound of Formula (I) or a form thereof that inhibits Bmi-1 function in the cell and subsequently administering the effective amount of the compound of Formula (I) or a form thereof to the subject.
Another embodiment described herein is directed to a method of inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in
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PCT/US2013/071132 need thereof comprising administering to the subject an effective amount of the compound of Formula (I) or a form thereof.
Another embodiment described herein is directed to a method for treating a cancer mediated by Bmi-1 in a subject in need thereof comprising contacting a cell having elevated Bmi-1 levels from the subject with an amount of a compound of Formula (I) or a form thereof, wherein the cell is selected from a cancer cell, tumor cell, cancer stem cell or tumor stem cell.
Another embodiment described herein is directed to a method further comprising contacting a cell having elevated Bmi-1 levels from the subject with an amount of the compound of Formula (I) or a form thereof, wherein the cell is selected from a cancer cell, tumor cell, cancer stem cell or tumor stem cell, determining an effective amount of the compound of Formula (I) or a form thereof that inhibits Bmi-1 function in the cell and subsequently administering the effective amount of the compound of Formula (I) or a form thereof to the subject.
Another embodiment described herein is directed to a method wherein the effective amount of the compound of Formula (I) or a form thereof determined to inhibit Bmi-1 function in the contacted cell reduces Bmi-1 levels in the contacted cell.
An embodiment of the method described herein comprises administering an effective amount of a compound of Formula (I) or a form thereof to inhibit the function of Bmi-1 in a cancer cell in vivo or in vitro, in a tumor cell in vivo or in vitro, in a cancer stem cell population in vivo or in vitro, or in a tumor stem population in vivo or in vitro.
An embodiment of the method described herein comprises administering an effective amount of a compound of Formula (I) or a form thereof to reduce the level of Bmi-1 in a cancer cell in vivo or in vitro, in a tumor cell in vivo or in vitro, in a cancer stem cell population in vivo or in vitro, or in a tumor stem population in vivo or in vitro.
An embodiment of the method described herein comprises administering an effective amount of a compound of Formula (I) or a form thereof to inhibit cancer cell proliferation, tumor cell proliferation, cancer stem cell proliferation or tumor stem cell proliferation.
An embodiment described herein includes the use of a compound of Formula (I) or a form thereof in the manufacture of a medicament for inhibiting Bmi-1 function and reducing
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PCT/US2013/071132 the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising administering an effective amount of the medicament to the subject.
Without being limited by theory, any type of cancer mediated by or dependent on the presence of overexpressed Bmi-1 can be treated in accordance with the intended use of the compounds of Formula (I) or a form thereof described herein.
As used herein, the term “cancer” refers to cells in which Bmi-1 is aberrantly expressed or overexpressed and the cell depends on Bmi-1 for survival or proliferation. Without being limited by theory, the cells may be either stem-like or more differentiated, but the cell relies on Bmi-1 to enable uncontrolled cell division and develop resistance to cytotoxic, chemotherapeutic agents.
In another embodiment, the term “a cancer mediated by Bmi-1” refers to a cancer that is characterized by cells or a fraction of cells from a cancer patient that overexpress Bmi-1 compared to cells from a cancer-free patient (i.e., a patient with no detectable cancer as determined by conventional techniques, such as MRI, CAT scan, etc.). Alternatively, the term refers to cells or a fraction of cells from a cancer patient that, relative to the cancer patient’s cells from surrounding normal tissues, express a level of Bmi-1 that differs by at least 2%, 4%, 8%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%. 90%, or 95% more, as detected by any method routinely used in the art, or described herein, e.g., in an ELISA.
Non-limiting examples of a cancer mediated by Bmi-1 that can be treated with the intended use described herein: leukemias, such as but not limited to, acute leukemia, acute lymphocytic leukemia, acute myelocytic leukemias, such as, myeloblastic, promyelocytic, myelomonocytic, monocytic, and erythroleukemia leukemias and myelodysplastic syndrome; chronic leukemias, such as but not limited to, chronic myelocytic (granulocytic) leukemia, chronic lymphocytic leukemia, hairy cell leukemia; polycythemia vera; lymphomas such as but not limited to Hodgkin’s lymphoma, non-Hodgkin’s lymphoma; multiple myelomas such as but not limited to smoldering multiple myeloma, nonsecretory myeloma, osteosclerotic myeloma, placancer cell leukemia, solitary placancercytoma and extramedullary placancercytoma; Waldenstrom’s macroglobulinemia; monoclonal gammopathy of undetermined significance; benign monoclonal gammopathy; heavy chain disease; bone and connective tissue sarcomas such as but not limited to bone sarcoma, osteosarcoma,
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PCT/US2013/071132 chondrosarcoma, Ewing’s sarcoma, malignant giant cell tumor, fibrosarcoma of bone, chordoma, periosteal sarcoma, soft-tissue sarcomas, angiosarcoma (hemangiosarcoma), fibrosarcoma, Kaposi’s sarcoma, leiomyosarcoma, liposarcoma, lymphangiosarcoma, neurilemmoma, rhabdomyosarcoma, synovial sarcoma; glial brain tumors (i.e., gliomas) such as but not limited to, astrocytoma, ependymoma, oligodendroglioma, brain stem glioma, optic glioma, diffuse intrinsic pontine glioma, mixed glioma (i.e., oligoastrocytoma), glioblastoma, glioblastoma multiforme, nonglial tumor, acoustic neurinoma, craniopharyngioma, medulloblastoma, meningioma, pineocytoma, pineoblastoma, primary brain lymphoma; breast cancer including but not limited to ductal carcinoma, adenocarcinoma, lobular (cancer cell) carcinoma, intraductal carcinoma, medullary breast cancer, mucinous breast cancer, tubular breast cancer, papillary breast cancer, Paget’s disease, and inflammatory breast cancer; adrenal cancer such as but not limited to pheochromocytom and adrenocortical carcinoma; thyroid cancer such as but not limited to papillary or follicular thyroid cancer, medullary thyroid cancer and anaplastic thyroid cancer; pancreatic cancer such as but not limited to, insulinoma, gastrinoma, glucagonoma, vipoma, somatostatin-secreting tumor, and carcinoid or islet cell tumor; pituitary cancers such as but limited to Cushing’s disease, prolactin-secreting tumor, acromegaly, and diabetes insipius; eye cancers such as but not limited to ocular melanoma such as iris melanoma, choroidal melanoma, and cilliary body melanoma, and retinoblastoma; vaginal cancers such as squamous cell carcinoma, adenocarcinoma, and melanoma; vulvar cancer such as squamous cell carcinoma, melanoma, adenocarcinoma, basal cell carcinoma, sarcoma, and Paget’s disease; cervical cancers such as but not limited to, squamous cell carcinoma, and adenocarcinoma; uterine cancers such as but not limited to endometrial carcinoma and uterine sarcoma; ovarian cancers such as but not limited to, ovarian epithelial carcinoma, borderline tumor, germ cell tumor, and stromal tumor; esophageal cancers such as but not limited to, squamous cancer, adenocarcinoma, adenoid cystic carcinoma, mucoepidermoid carcinoma, adenosquamous carcinoma, sarcoma, melanoma, placancercytoma, verrucous carcinoma, and oat cell (cancer cell) carcinoma; stomach cancers such as but not limited to, adenocarcinoma, fungating (polypoid), ulcerating, superficial spreading, diffusely spreading, malignant lymphoma, liposarcoma, fibrosarcoma, and carcinosarcoma; colon cancers; rectal cancers; liver cancers such as but not limited to hepatocellular carcinoma and hepatoblastoma; gallbladder cancers such as adenocarcinoma; cholangiocarcinomas such as but not limited to papillary, nodular, and diffuse; lung cancers
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PCT/US2013/071132 such as non-small cell lung cancer, squamous cell carcinoma (epidermoid carcinoma), adenocarcinoma, large-cell carcinoma and small-cell lung cancer; testicular cancers such as but not limited to germinal tumor, seminoma, anaplastic, classic (typical), spermatocytic, nonseminoma, embryonal carcinoma, teratoma carcinoma, choriocarcinoma (yolk-sac tumor), prostate cancers such as but not limited to, prostatic intraepithelial neoplasia, adenocarcinoma, leiomyosarcoma, and rhabdomyosarcoma; penal cancers; oral cancers such as but not limited to squamous cell carcinoma; basal cancers; salivary gland cancers such as but not limited to adenocarcinoma, mucoepidermoid carcinoma, and adenoidcystic carcinoma; pharynx cancers such as but not limited to squamous cell cancer, and verrucous; skin cancers such as but not limited to, basal cell carcinoma, squamous cell carcinoma and melanoma, superficial spreading melanoma, nodular melanoma, lentigo malignant melanoma, acral lentiginous melanoma; kidney cancers such as but not limited to renal cell carcinoma, adenocarcinoma, hypernephroma, fibrosarcoma, transitional cell cancer (renal pelvis and/ or uterer); Wilms’ tumor; bladder cancers such as but not limited to transitional cell carcinoma, squamous cell cancer, adenocarcinoma, carcinosarcoma. In addition, cancers include myxosarcoma, osteogenic sarcoma, endotheliosarcoma, lymphangioendotheliosarcoma, mesothelioma, synovioma, hemangioblastoma, epithelial carcinoma, cystadenocarcinoma, bronchogenic carcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma and papillary adenocarcinomas (for a review of such disorders, see Fishman et al., 1985, Medicine, 2d Ed., J.B. Lippincott Co., Philadelphia and Murphy et al., 1997, Informed Decisions: The Complete Book of Cancer Diagnosis, Treatment, and Recovery, Viking Penguin, Penguin Books U.S.A., Inc., United States of America).
The compounds of Formula (I) or a form thereof are also useful in the treatment, prevention and/or management of a variety of cancers mediated by Bmi-1 or other abnormal proliferative diseases (where such disease is mediated by overexpressed Bmi-1 or elevated levels of Bmi-1), including (but not limited to) the following: carcinoma, including that of the bladder, breast, colon, kidney, liver, lung, ovary, pancreas, stomach, cervix, thyroid and skin; including squamous cell carcinoma; hematopoietic tumors of lymphoid lineage, including leukemia, acute lymphocytic leukemia, acute lymphoblastic leukemia, B-cell lymphoma, T cell lymphoma, Burkitt’s lymphoma; hematopoietic tumors of myeloid lineage, including acute and chronic myelogenous leukemias and promyelocytic leukemia; tumors of mesenchymal origin, including fibrosarcoma and rhabdomyoscarcoma; other tumors,
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PCT/US2013/071132 including melanoma, seminoma, tetratocarcinoma, neuroblastoma; tumors of the central and peripheral nervous system, including astrocytoma, neuroblastoma, glioma, and Schwannomas; tumors of mesenchymal origin, including fibrosarcoma, rhabdomyoscarama, and osteosarcoma; and other tumors, including melanoma, xeroderma pigmentosum, keratoactanthoma, seminoma, thyroid follicular cancer and teratocarcinoma. In some embodiments, cancers associated with aberrations in apoptosis are treated in accordance with the methods described herein. Such cancers may include, but are not limited to, follicular lymphomas, carcinomas with p53 mutations, hormone dependent tumors of the breast, prostate and ovary, and precancerous lesions such as familial adenomatous polyposis, and myelodysplastic syndromes. In specific embodiments, malignancy or dysproliferative changes (such as metaplasias and dysplasias), or hyperproliferative disorders of the skin, lung, liver, bone, brain, stomach, colon, breast, prostate, bladder, kidney, pancreas, ovary, and/or uterus are treated in accordance with the methods described herein. In other specific embodiments, a sarcoma, or melanoma is treated as described herein.
In a specific embodiment, the cancer mediated by Bmi-1 being treated as described herein is leukemia, lymphoma or myeloma (e.g., multiple myeloma). Non-limiting examples of leukemias and other blood-borne cancers mediated by Bmi-1 that can be treated with the methods described herein include acute lymphoblastic leukemia (ALL), acute lymphoblastic B-cell leukemia, acute lymphoblastic T-cell leukemia, acute myeloblastic leukemia (AML), acute promyelocytic leukemia (APL), acute monoblastic leukemia, acute erythroleukemic leukemia, acute megakaryoblastic leukemia, acute myelomonocytic leukemia, acute nonlymphocyctic leukemia, acute undifferentiated leukemia, chronic myelocytic leukemia . (CML), chronic lymphocytic leukemia (CLL), and hairy cell leukemia.
Non-limiting examples of lymphomas mediated by Bmi-1 that can be treated in accordance with the methods described herein include Hodgkin’s lymphoma, non-Hodgkin’s lymphoma, multiple myeloma, Waldenstrom’s macroglobulinemia, heavy chain disease, and polycythemia vera.
In another embodiment, the cancer mediated by Bmi-1 being treated as described herein is a solid tumor. Examples of solid tumors that can be treated in accordance with the methods described herein include, but are not limited to fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma,
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PCT/US2013/071132 endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing’s tumor, leiomyosarcoma, rhabdomyosarcoma, colon cancer, colorectal cancer, kidney cancer, pancreatic cancer, bone cancer, breast cancer, ovarian cancer, prostate cancer, esophageal cancer, stomach cancer, oral cancer, nasal cancer, throat cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilms’ tumor, cervical cancer, uterine cancer, testicular cancer, small cell lung carcinoma, bladder carcinoma, lung cancer, epithelial carcinoma, glioma, glioblastoma multiforme, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, meningioma, skin cancer, melanoma, neuroblastoma, and retinoblastoma.
In certain embodiments, a cancer mediated by Bmi-1 includes, but is not limited to, brain cancer, gastric cancer, hematologic cancer, lung cancer, non-small cell lung cancer, pancreatic cancer, prostate cancer, salivary gland cancer, colorectal carcinoma, hepatocellular carcinoma, liver carcinoma, breast carcinomas or sarcomas, esophageal carcinomas or sarcomas, stomach carcinomas or sarcomas, fibrosarcoma, glioblastoma, diffuse intrinsic pontine glioma, medulloblastoma, neuroblastoma, diffuse large B cell lymphomas, B cell non-Hodgkin’s lymphoma, Hodgkin’s lymphoma or chronic or acute myeloid leukemia.
In certain embodiments, a cancer mediated by Bmi-1 includes, but is not limited to, tumors that relapse after therapy despite improved surgical and irradiation techniques. Tumor relapse may occur for a number of reasons, with one plausible explanation being the existence of cancer stem cells (CSC) or tumor stem cells (tumor initiating cells) in the tumor population. CSCs are defined as a population of stem cells relative to any type of blood cancer, solid tumor cancer or metastatic cancer. Tumor stem cells are those specifically found within a tumor. Both have characteristics similar to normal stem cells. Like normal stem cells, CSCs and tumor stem cells have the potential to self renew. Unlike normal stem cells, though, due to the sustained presence of high levels of Bmi-1, the CSCs and tumor stem cells fail to terminally differentiate and proliferate unchecked. Their enhanced DNA repair capacity also enables them to become resistant to cytotoxic, chemotherapeutic drugs designed to kill cancer cells and tumor cells. Therefore, targeting CSCs and tumor stem cells that
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PCT/US2013/071132 overexpress Bmi-1 could be an approach for effective cancer treatment. One further approach is to target various transcription factors responsible for maintenance of the self renewal capacity of CSCs and tumor stem cells.
As used herein, the term “treat,” “treatment” or “treating” refers to: (i) preventing a disease, disorder and/or condition from occurring in a subject that may be predisposed to the disease, disorder and/or condition but has not yet been diagnosed as having said disease, disorder and/or condition; (ii) inhibiting a disease, disorder and/or condition, i.e., arresting its development; and/or (iii) relieving a disease, disorder and/or condition, i.e., causing regression of the disease, disorder and/or condition.
As used herein, the term “subject” refers to members of the human, equine, porcine, bovine, murine, rattus, canine and feline species. In some embodiments, the subject is a mammal or a warm-blooded vertebrate animal. In other embodiments, the subject is a human. As used herein, the term “patient” may be used interchangeably with “subject” and “human”.
In certain embodiments, the subject is a human that is 0 to 6 months old, 6 to 12 months old, 6 to 18 months old, 18 to 36 months old, 1 to 5 years old, 5 to 10 years old, 10 to 15 years old, 15 to 20 years old, 20 to 25 years old^ 25 to 30 years old, 30 to 35 years old, 35 to 40 years old, 40 to 45 years old, 45 to 50 years old, 50 to 55 years old, 55 to 60 years old, 60 to 65 years old, 65 to 70 years old, 70 to 75 years old, 75 to 80 years old, 80 to 85 years old, 85 to 90 years old, 90 to 95 years old or 95 to 100 years old. In some embodiments, the subject is a human infant. In other embodiments, the subject is a human toddler. In other embodiments, the subject is a human child. In other embodiments, the subject is human adult. In yet other embodiments, the subject is an elderly human.
As used herein, the term “elderly human” refers to a human 65 years or older; the term “human adult” refers to a human that is 18 years or older; the term “human child” refers to a human that is 1 year to 18 years old; the term “human infant” refers to a newborn to 1 year old year human; and, the term “human toddler” refers to a human that is 1 year to 3 years old.
In certain embodiments, the subject is in an immunocompromised state or immunosuppressed state or at risk for becoming immunocompromised or immunosuppressed.
In certain embodiments, the subject is receiving or recovering from an immunosuppressive
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PCT/US2013/071132 therapy. In certain embodiments, the subject has or is at risk of getting cancer, AIDS, or a bacterial infection. In certain embodiments, the subject is, will or has undergone surgery, chemotherapy and/or radiation therapy. In certain embodiments, the subject has cystic fibrosis, pulmonary fibrosis or another condition affecting the lungs. In certain embodiments, the subject has, will have or had a tissue transplant.
In some embodiments, the subject's cancer, due to the overexpression of Bmi-1 in cancer cells, tumor cells, cancer stem cells or tumor stem cells thereof, has proven refractory to conventional standard of care therapies (excluding treatment with a compound of Formula (I) or a form thereof), such that the patient has discontinued the conventional therapy. In one embodiment, without being limited by theory, the term refractory means that at least some significant portion of the cancer cells, tumor cells, cancer stem cells or tumor stem cells continue to proliferate due to the overexpression of Bmi-1, despite therapy. The determination of whether the cancer is refractory toa particular therapy can be made either in vivo or in vitro by any method known in the art for assaying the effect of a therapy on the cancer cells, tumor cells, cancer stem cells or tumor stem cells, using the art-accepted meanings of “refractory” in such a context. In certain embodiments, a patient having a refractory cancer due to the overexpression of Bmi-1 is a patient in which the cancer is nonresponsive or resistant to a conventional or standard of care therapy. In certain embodiments, a patient with refractory cancer has a cancer mediated by Bmi-1 that progresses. Disease progression, as a lack of clinical response to a therapy, is demonstrated when the tumor or neoplasm has not been significantly eradicated and/or the symptoms have not been significantly alleviated. The determination of whether a patient has a refractory cancer mediated by Bmi-1 can be made either in vivo or in vitro by any method known in the art for assaying the effectiveness of the therapy for the treatment of the cancer, using artaccepted meanings of “refractory” in such a context.
In certain embodiments, the patient to be treated in accordance with the methods described herein is a patient already being treated with antibiotics, anti-virals, anti-fungals, or other biological therapy, immunotherapy or anti-cancer therapy. Among these patients are patients with a refractory cancer mediated by Bmi-1 or patients too young for conventional therapies. In some embodiments, the patient being treated is treatment naive, not having received any prior therapy. In any of the foregoing embodiments, a patient to be treated may receive a small molecule therapy.
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In some embodiments, a compound of Formula (I) or a form thereof may be prophylactically administered to a patient to prevent the onset of cancer mediated by Bmi-1 in a patient at risk of developing cancer. In some embodiments, a compound of Formula (I) or a form thereof may be therapeutically administered to a patient that is susceptible to adverse reactions to conventional therapies. In some embodiments, the subject being administered one or more compounds of Formula (I) or a form thereof has not received prior therapy. In other embodiments, one or more compounds of Formula (I) or a form thereof are administered to a subject who has received a prior therapy. In some embodiments, the subject administered a compound of Formula (I) or a form thereof has discontinued a prior therapy due to lack of benefit from the therapy, adverse effects from the therapy or unacceptable levels of toxicity.
In some embodiments, the subject being administered one or more compounds of Formula (I) or a form thereof, will or has undergone surgery, chemotherapy, antibody therapy, hormonal therapy and/or radiation therapy. In certain embodiments, the patient has undergone surgery to remove the tumor or neoplasm. In certain embodiments, the subject will have, or has had, or is undergoing a tissue or organ transplant.
As used herein, the terms “effective amount,” “prophylactically effective amount” or therapeutically effective amount mean an amount of a compound of Formula (I) or a form thereof that is effective in inhibiting Bmi-1 protein function and reducing the level of Bmi-1 protein, as described herein, and thus producing the desired prophylactic, therapeutic, ameliorative, inhibitory or preventative effect in a cancer mediated by Bmi-1 in a patient in need thereof.
As used herein, the term “effective amount,” in the context of administering a compound of Formula (I) or a form thereof to a patient, refers to the amount of a compound of Formula (I) or a form thereof which is sufficient to achieve at least one or more of the following effects, as applicable, in a patient or in patient cell(s): (i) inhibition of Bmi-1 protein function; (ii) reduction in the level or quantity of Bmi-1 protein; (iii) reduction or amelioration in the severity of a cancer mediated by Bmi-1 or a symptom associated therewith; (iv) prevention of the progression of a cancer mediated by Bmi-1 or a symptom associated therewith; (v) regression of a cancer mediated by Bmi-1 or a symptom associated therewith; (vi) prevention of the development or onset of a cancer mediated by Bmi-1 or a
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PCT/US2013/071132 symptom associated therewith; (vii) prevention of the recurrence of a cancer mediated by Bmi-1 or a symptom associated with a cancer mediated by Bmi-1; (viii) reduction of the duration of a symptom associated with a cancer mediated by Bmi-1; (ix) reduction or elimination of the cancer stem cell or tumor stem cell population; (x) reduction or elimination of the growth of a tumor or neoplasm overexpressing Bmi-1; (xi) reduction or elimination of the proliferation of cancer cells or tumor cells; (xii) reduction or elimination of the formation of a tumor or neoplasm overexpressing Bmi-1; (xiii) eradication or control of a primary, regional and/or metastatic cancer mediated by Bmi-1; (xiv) reduction in patient mortality; (xv) increased number of patients in remission; (xvi) increased length of remission in patients; (xvii) the size of a tumor or neoplasm overexpressing Bmi-1 is maintained or controlled such that the size does not increase or increases less than the size of the tumor after administration of a standard therapy as measured by conventional methods available to one of skill in the art, such as MRI, X-ray and CAT scan; (xviii) increased delay in disease progression; (xix) increased patient survival; (xx) reduction in incidences of patient hospitalization; (xxi) reduction in the length of patient hospitalization; (xxii) enhancement or improvement in the prophylactic or therapeutic effect(s) of another therapy; (xxiii) reduction in the number of symptoms associated with a cancer mediated by Bmi-1; (xxiv) increased cancer-free survival of patients; and/or (xxv) increased symptom-free survival of cancer patients.
In general, the term “effective amount” also includes that amount of a compound of Formula (I) or a form thereof administered to a patient which is in a range of from about 0.001 mg/Kg/day to about 500 mg/Kg/day, or about 0.01 mg/Kg/day to about 500 mg/Kg/day, or about 0.1 mg to about 500 mg/Kg/day, or about 1.0 mg/day to about 500 mg/Kg/day, in single, divided, or a continuous dose for a patient or subject having a weight in a range of between about 40 to about 200 Kg (which dose may be adjusted for patients or subjects above or below this range, particularly children under 40 Kg). The typical adult subject is expected to have a median weight in a range of between about 60 to about 100 Kg. The effective amount for the subject will also depend upon various factors, including the body weight, size and health of the subject. An effective amount for a given patient can be determined according to the skill and judgment of the clinician.
In another embodiment, where daily doses are adjusted based upon the weight of the subject or patient, compounds of Formula (I) or a form thereof described herein may be
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PCT/US2013/071132 formulated for delivery at about 0.02, 0.025, 0.03, 0.05, 0.06, 0.075, 0.08, 0.09, 0.10, 0.20, 0.25,0.30, 0.50, 0.60, 0.75,0.80, 0.90, 1.0, 1.10, 1.20, 1.25, 1.50, 1.75,2.0,5.0, 10, 20 or 50 mg/Kg/day. Daily doses adjusted based upon the weight of the subject or patient may be administered as a single, divided, or continuous dose. In embodiments where a dose of a compound of Formula (I) or a form thereof is given more than once per day, the dose may be administered once, twice, three times, or more per day. In another embodiment, a subject is administered one or more doses of an effective amount of a compound of Formula (I) or a form thereof, wherein the effective amount may not be the same for each dose.
Another embodiment described herein iincludes an effective amount of the compound of Formula (I) or a form thereof in a range of from about 0.001 mg/Kg/day to about 500 mg/Kg/day.
Within the scope described herein, the “effective amount” of a compound of Formula (I) or a form thereof for use in the manufacture of a medicament or in a method for treating a cancer mediated by Bmi-1 in a subject in need thereof, is intended to include an amount in a range of from about 0.1 ng to about 3500 mg administered daily; from about 0.1 μg to about 3500 mg administered daily; from about 0.1 mg to about 3500 mg administered daily; from about 1 mg to about 3500 mg administered daily; from about 1 mg to about 3000 mg administered daily; from about 0.05 mg to about 1500 mg administered daily; from about 0.5 mg to about 1500 mg administered daily; from about 1 mg to about 1500 mg administered daily; from about 5 mg to about 1500 mg administered daily; from about 10 mg to about 600 mg administered daily; from about 0.5 mg to about 2000 mg administered daily; or, an amount in a range of from about 5.0 mg to about 1500 mg administered daily.
Another embodiment described herein iincludes an effective amount of the compound of Formula (I) or a form thereof in a range of from about 0.1 ng to about 3500 mg.
For any compound of Formula (I) or a form thereof, the effective amount can be estimated initially by results from cell culture assays or from relevant animal models, such as the mouse, chimpanzee, marmoset or tamarin animal model. Relevant animal models may also be used to determine the appropriate concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans. Therapeutic efficacy and toxicity may be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., ED50 (the dose therapeutically
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PCT/US2013/071132 effective in 50% of the population) and LD50 (the dose lethal to 50% of the population). The dose ratio between the toxic and therapeutic effect is referred to as the therapeutic index, and can be expressed as the ratio, LD50/ED50. In some embodiments, the effective amount is such that a large therapeutic index is achieved. In further embodiments, the dosage is within a range of plasma concentrations that include an ED50 with little or no toxicity. The dosage may vary within this range depending upon the dosage form employed, sensitivity of the patient, and the route of administration.
More specifically, the concentration-biological effect (pharmacodynamic) relationship observed with regard to a compound of Formula (I) or a form thereof suggests a target plasma concentration ranging from about 0.001 pg/mL to about 50 pg/mL, from about 0.01 pg/mL to about 20 pg/mL, from about 0.05 pg/mL to about 10 pg/mL, or from about 0.1 pg/mL to about 5 pg/mL. To achieve such plasma concentrations, the compounds of Formula (I) or a form thereof described herein may be administered at doses that vary from 0.001 pg to 100,000 mg, depending upon the route of administration in single, divided, or continuous doses for a patient weighing between about 40 to about 100 kg (which dose may be adjusted for patients above or below this weight range, particularly for children under 40 kg).
The exact dosage will be determined by the practitioner, in light of factors related to the subject. Dosage and administration may be adjusted to provide sufficient levels of the active agent(s) or to maintain the desired effect. Administration factors that may be taken into account include the severity of the disease state, general health of the subject, ethinicity, age, weight, and gender of the subject, diet, time and frequency of administration, drug combination(s), reaction sensitivities, tolerance for toxicity related to drug metabolites, experience with other cancer therapies and regimens, and tolerance/response to such therapies and regimens. Long-acting pharmaceutical compositions may be administered every 2, 3 or 4 days, once every week, or once every two weeks depending on half-life and clearance rate of the particular formulation.
The compounds of Formula (I) or a form thereof described herein may be administered to the subject via any drug delivery route known in the art. Nonlimiting examples include oral, ocular, rectal, buccal, topical, nasal, ophthalmic, subcutaneous, intramuscular, intraveneous (bolus and infusion), intracerebral, transdermal, and pulmonary routes of administration.
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Compound Metabolites
Also falling within the scope described herein are the in vivo metabolic products of the compounds of Formula (I) or a form thereof. Such products may result, for example, from the oxidation, reduction, hydrolysis, amidation, glucuronidation, esterification and the like of the administered compound of Formula (I) or a form thereof, primarily due to enzymatic processes. Accordingly, the compounds of Formula (I) or a form thereof described herein include those produced by a process comprising contacting a compound of Formula (I) or a form thereof described herein with a mammalian tissue or a mammal for a period of time sufficient to yield a metabolic product thereof.
Such products typically are identified by preparing a radio-labeled (e.g. C14 or H3) compound of Formula (I) or a form thereof described herein, administering it in a detectable dose (e.g., greater than about 0.5 mg/kg) to a mammal such as rat, mouse, guinea pig, monkey, or to man, allowing sufficient time for metabolism to occur (typically about 30 seconds to 30 hours), and isolating its conversion products from urine, blood or other biological samples. These products are easily isolated since they are labeled (others are isolated by the use of antibodies capable of binding epitopes surviving in the metabolite). The metabolite structures are determined in conventional fashion, e.g., by MS or NMR analysis. In general, analysis of metabolites may be done in the same way as conventional drug metabolism studies well-known to those skilled in the art. The conversion products, so long as they are not otherwise found in vivo, are useful in diagnostic assays for therapeutic dosing of the compounds of Formula (I) or a form thereof described herein even if they possess no biological activity of their own.
Combination Therapies
The methods of treating a cancer mediated by Bmi-1 in a subject in need thereof, in addition to those previously described herein, further comprise administering to the subject in need thereof an effective amount of one or more of the compounds of Formula (I) or a form thereof alone or in combination with one or more additional agents selected from anti-cancer agents, anti-proliferative agents, chemotherapeutic agents, immunomodulatory agents, antiangiogenic agents, anti-inflammatory agents, an alkylating agents, steroidal and non-steriodal anti-inflammatory agents, pain relievers, leukotriene antagonists, p)2-agonists, anticholinergic agents, hormonal agents, biological agents, tubulin binding agents, glucocorticoids,
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PCT/US2013/071132 corticosteroid agents, antibacterial agents, antihistamines, anti-malarial agents, anti-viral agents, antibiotics and the like; and, optionally with radiation therapy.
In another embodiment, one or more compounds of Formula (I) or a form thereof alone or in combination with one or more additional agents may be administered to the subject in combination with a supportive therapy, a pain relief therapy, or other therapy that does not have an effect on a cancer mediated by Bmi-1.
In some embodiments, one or more compounds of Formula (I) or a form thereof described herein and one or more additional agents described herein are administered as the same pharmaceutical composition. In certain embodiments, one or more compounds of Formula (I) or a form thereof described herein and one or more additional agents described herein are administered in different pharmaceutical compositions. In certain embodiments, one or more compounds of Formula (I) or a form thereof described herein and one or more additional agents described herein are administered by the same route of administration. In certain embodiments, one or more compounds of Formula (I) or a form thereof described herein and one or more additional agents described herein are administered by different routes of administration.
In other embodiments are pharmaceutical compositions wherein one or more compounds of Formula (I) or a form thereof are administered in a combination product with one or more additional agents useful in the treatment of a cancer mediated by Bmi-1. The skilled artisan will recognize that a variety of active ingredients may be administered in a combination with the compounds of Formula (I) or a form thereof described herein whereby the product may act to augment or synergistically enhance the anticancer activity of either or both the additional agent(s) and the compound(s) of Formula (I) or a form thereof described herein.
As used herein, the term “synergistic,” refers to the effect of the administration of a combination product as described herein which is more effective than the additive effects of any two or more single agents. In a specific embodiment, a synergistic effect of a combination product permits the use of lower dosages of one or more agents and/or less frequent administration of said agents to a subject with a cancer mediated by Bmi-1. In certain embodiments, the ability to utilize lower dosages of an agent and/or to administer said agents less frequently reduces the toxicity associated with the administration of said agents to
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PCT/US2013/071132 a subject without reducing the efficacy of said agents in the prevention or treatment of a cancer mediated by Bmi-1. In some embodiments, a synergistic effect results in improved efficacy of each of the agents in treating a cancer mediated by Bmi-1. In some embodiments, a synergistic effect of a combination of agents avoids or reduces adverse or unwanted side effects associated with the use of any single agent. The combination of agents in such a product can be administered to a subject in the same pharmaceutical composition. Alternatively, the agents can be administered concurrently to a subject in separate pharmaceutical compositions. The agents may also be administered to a subject by the same or different routes of administration. In a specific embodiment, at least one of the agents is a compound of Formula (I) or a form thereof described herein.
It is also possible to combine any compound of Formula (I) or a form thereof described herein with such additional agents useful in the treatment of a cancer mediated by Bmi-1, including compounds of Formula (I) or a form thereof as described herein, in a unitary dosage form, or in separate dosage forms intended for simultaneous or sequential administration to a patient in need of treatment. When administered sequentially, the combination may be administered in two or more administrations. In an alternative embodiment, it is possible to administer one or more compounds of Formula (I) or a form thereof described herein and one or more additional agents described herein by different routes.
According to the methods described herein, a combination product may include a combination of active ingredients that may be: (1) co-formulated and administered or delivered simultaneously in a combined formulation; (2) delivered sequentially or in parallel as separate formulations; or (3) by any other combination regimen known in the art. When delivered as separate formulations in alternation therapy, the methods described herein may comprise administration or delivery, for example, without limitation, in separate solutions, emulsions, suspensions, tablets, pills or capsules, or by different injections in separate syringes. In general, when administered in alternation, an effective dosage of each active ingredient is administered serially, one dose following another. In contrast, in parallel or simultaneous administration, effective dosages of two or more active ingredients are administered together. Various alternative combinations of intermittent sequential or in parallel combination administration may also be used.
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Specific examples of such agents include, but are not limited to, immunomodulatory agents (e.g., interferon, penicillamine and the like), anti-angiogenic agent, anti-inflammatory agents (e.g., adrenocorticoids, corticosteroids (e.g., beclomethasone, budesonide, flunisolide, fluticasone, triamcinolone, methylprednisolone, prednisolone, prednisone, hydrocortisone), glucocorticoids, steroidal and non-steriodal anti- inflammatory drugs (e.g., aspirin, ibuprofen, diclofenac, and COX-2 inhibitors)), pain relievers, leukotriene antagonists (e.g., montelukast, methyl xanthines, zafirlukast, and zileuton), [32-agonists (e.g., albuterol, biterol, fenoterol, isoetharie, metaproterenol, pirbuterol, salbutamol, terbutalin formoterol, salmeterol, and salbutamol terbutaline), anticholinergic agents (e.g., ipratropium bromide and oxitropium bromide), antibacterial agents (e.g., sulphasalazine, dapsone and the like), antihistamines, anti-malarial agents (e.g., hydroxychloroquine), anti-viral agents (e.g., nucleoside analogs (e.g., zidovudine, acyclovir, gangcyclovir, vidarabine, idoxuridine, trifluridine, ribavirin, foscamet, amantadine, rimantadine, saquinavir, indinavir, ritonavir, and AZT) and antibiotics (e.g., dactinomycin (formerly actinomycin), bleomycin, erythomycin, penicillin, mithramycin, and anthramycin (AMC)).
Specific examples of additional agents that may be used in combination with a compound of Formula (I) or a form thereof described herein include, but are not limited to: acivicin; aclarubicin; acodazole hydrochloride; acronine; adozelesin; aldesleukin; altretamine; ambomycin; ametantrone acetate; aminoglutethimide; amsacrine; anastrozole; anthracyclin; anthramycin; asparaginase; asperlin; azacitidine; azetepa; azotomycin; batimastat; benzodepa; bicalutamide; bisantrene hydrochloride; bisnafide dimesylate; bisphosphonates (e.g., pamidronate (Aredria®), sodium clondronate (Bonefos®), zoledronic acid (Zometa®), alendronate (Fosamax®), etidronate, ibandornate, cimadronate, risedromate, and tiludromate); bizelesin; bleomycin sulfate; brequinar sodium; bropirimine; busulfan; cactinomycin; calusterone; caracemide; carbetimer; carboplatin; carmustine; carubicin hydrochloride; carzelesin; cedefingol; chlorambucil; cirolemycin; cisplatin; cladribine; crisnatol mesylate; cyclophosphamide; cytarabine; dacarbazine; dactinomycin; daunorubicin hydrochloride; decitabine; demethylation agents; dexormaplatin; dezaguanine; dezaguanine mesylate; diaziquone; docetaxel; doxorubicin; doxorubicin hydrochloride; droloxifene; droloxifene citrate; dromostanolone propionate; duazomycin; edatrexate; eflomithine hydrochloride; EphA2 inhibitors; elsamitrucin; enloplatin; enpromate; epipropidine; epirubicin hydrochloride; erbulozole; esorubicin hydrochloride; estramustine; estramustine
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PCT/US2013/071132 phosphate sodium; etanidazole; etoposide; etoposide phosphate; etoprine; fadrozole hydrochloride; fazarabine; fenretinide; floxuridine; fludarabine phosphate; 5-fluorouracil; fluorocitabine; fosquidone; fostriecin sodium; gemcitabine; gemcitabine hydrochloride; histone deacetylase inhibitors; hydroxyurea; idarubicin hydrochloride; ifosfamide; ilmofosine; imatinib mesylate; interleukin II (including recombinant interleukin II, or rIL2), interferon alpha-2a; interferon alpha-2b; interferon alpha-nl ; interferon alpha-n3; interferon beta-I a; interferon gamma-I b; iproplatin; irinotecan hydrochloride; lanreotide acetate; lenalidomide; letrozole; leuprolide acetate; liarozole hydrochloride; lometrexol sodium; lomustine; losoxantrone hydrochloride; masoprocol; maytansine; mechlorethamine hydrochloride; anti-CD2 antibodies; megestrol acetate; melengestrol acetate; melphalan; menogaril; mercaptopurine; methotrexate; methotrexate sodium; metoprine; meturedepa; mitindomide; mitocarcin; mitocromin; mitogillin; mitomalcin; mitomycin; mitosper; mitotane; mitoxantrone hydrochloride; mycophenolic acid; nocodazole; nogalamycin; ormaplatin; oxisuran; paclitaxel; pegaspargase; peliomycin; pentamustine; peplomycin sulfate; perfosfamide; pipobroman; piposulfan; piroxantrone hydrochloride; plicamycin; plomestane; porfimer sodium; porfiromycin; prednimustine; procarbazine hydrochloride; puromycin; puromycin hydrochloride; pyrazofurin; riboprine; rogletimide; safmgol; safingol hydrochloride; semustine; simtrazene; sparfosate sodium; sparsomycin; spirogermanium hydrochloride; spiromustine; spiroplatin; streptonigrin; streptozocin; sulofenur; talisomycin; tecogalan sodium; tegafur; teloxantrone hydrochloride; temoporfin; teniposide; teroxirone; testolactone; thiamiprine; thioguanine; thiotepa; tiazofurin; tirapazamine; toremifene citrate; trestolone acetate; triciribine phosphate; trimetrexate; trimetrexate glucuronate; triptorelin; tubulozole hydrochloride; uracil mustard; uredepa; vapreotide; verteporfin; vinblastine sulfate; vincristine sulfate; vindesine; vindesine sulfate; vinepidine sulfate; vinglycinate sulfate; vinleurosine sulfate; vinorelbine tartrate; vinrosidine sulfate; vinzolidine sulfate; volitinib; vorozole; zeniplatin; zinostatin; zorubicin hydrochloride and the like.
Other examples of treating a cancer mediated by Bmi-1 include treatment with an anti-cancer or anti-proliferative agent wherein the anti-cancer or anti-proliferative agent is selected from, but not limited to: 20-Epi-l,25-dihydroxyvitamin D3 (MC 1288, MC 1301, KH 1060); 5-ethynyluracil; abiraterone; aclarubicin; acylfulvene; adecypenol; adozelesin; aldesleukin; ALL-TIC antagonists; altretamine; ambamustine; amidox; amifostine; aminolevulinic acid; amrubicin; amsacrine; anagrelide; anastrozole; andrographolide;
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PCT/US2013/071132 angiogenesis inhibitors; antagonist D; antagonist G; antarelix; anti-dorsalizing morphogenetic protein-1; antiandrogen, antiestrogen; antineoplaston; antisense oligonucleotides; aphidicolin glycinate; apoptosis gene modulators; apoptosis regulators; apurinic acid; ara-CDP-DLPTBA (0-palmitoyl-l-thioglycerol); arginine deaminase; asulacrine; atamestane; atrimustine; axinastatin 1; axinastatin 2; axinastatin 3; azasetron; azatoxin; azatyrosine; baccatin III derivatives; balanol; batimastat; BCR/ABL antagonists; benzochlorins; benzoylstaurosporine; beta lactam derivatives; beta-alethine; betaclamycin B; betulinic acid; bFGF inhibitor; bicalutamide; bisantrene; bisaziridinylspermine; bisnafide; bistratene A; bizelesin; breflate; bropirimine; budotitane; buthionine sulfoximine; calcipotriol; calphostin C; camptothecin derivatives; canarypox IL-2; capecitabine; carboxamide-amino-triazole (CaRest M3); CARN 700; cartilage derived inhibitor; carzelesin; casein kinase inhibitors (ICOS); castanospermine; cecropin B; cetrorelix; chlorins; chloroquinoxaline sulfonamide; cicaprost; cis-porphyrin; cladribine; clomifene analogues; clotrimazole; collismycin A; collismycin B; combretastatin A4; combretastatin analogue; conagenin; crambescidin 816; crisnatol; cryptophycin 8; cryptophycin A derivatives; curacin A; cyclopentanthraquinones; cycloplatam; cypemycin; cytarabine ocfosfate (YNK01 or Starasid®); cytolytic factor; cytostatin; dacliximab; decitabine; dehydrodidemnin B; deslorelin; dexamethasone; dexifosfamide; dexrazoxane; dexverapamil; diaziquone; didemnin B; didox; diethylnorspermine; dihydro-5-azacytidine; dihydrotaxol, dioxamycin; diphenyl spiromustine; docetaxel; docosanol; dolasetron; doxifluridine; droloxifene; dronabinol; duocarmycin SA; ebselen; ecomustine; edelfosine; edrecolomab; eflomithine; elemene; emitefur; epirubicin; epristeride; estramustine analogue; estrogen agonists; estrogen antagonists; etanidazole; etoposide phosphate; exCmestane; fadrozole; fazarabine; fenretinide; filgrastim; finasteride; flavopiridol; flezelastine; fluasterone; fludarabine; fluorodaunoruniein hydrochloride; forfenimex; formestane; fostriecin; fotemustine; gadolinium texaphyrin; gallium nitrate; galocitabine; ganirelix; gelatinase inhibitors; gemcitabine; glutathione inhibitors; HMG CoA reductase inhibitors (e.g., atorvastatin, cerivastatin, fluvastatin, lescol, lupitor, lovastatin, rosuvastatin, and simvastatin); hepsulfam; heregulin; hexamethylene bisacetamide; hypericin; ibandronic acid; idarubicin; idoxifene; idramantone; ilmofosine; ilomastat; imidazoacridones; imiquimod; immunostimulant peptides; insulin-like growth factor-1 receptor inhibitor; interferon agonists; interferons; interleukins; iobenguane; iododoxorubicin; ipomeanol, 4-iroplact; irsogladine; isobengazole; isohomohalicondrin B; itasetron; jasplakinolide; kahalalide F;
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PCT/US2013/071132 lamellarin-N triacetate; lanreotide; leinamycin; lenograstim; lentinan sulfate; leptolstatin; letrozole; leukemia inhibiting factor; leukocyte alpha interferon; leuprolide/estrogen/progesterone combinations; leuprorelin; levamisole; LFA-3TIP (see, International Publication No. WO93/0686 and U.S. Patent No. 6,162,432); liarozole; linear polyamine analogue; lipophilic disaccharide peptide; lipophilic platinum compounds; lissoclinamide 7; lobaplatin; lombricine; lometrexol; lonidamine; losoxantrone; lovastatin; loxoribine; lurtotecan; lutetium texaphyrin; lysofylline; lytic peptides; maitansine; mannostatin A; marimastat; masoprocol; maspin; matrilysin inhibitors; matrix metalloproteinase inhibitors; menogaril; merbarone; meterelin; methioninase; metoclopramide; MIF tautomerase inhibitor; mifepristone; miltefosine; mirimostim; mismatched double stranded RNA; mitoguazone; mitolactol; mitomycin analogues; mitonafide; mitotoxin fibroblast growth factor-saporin; mitoxantrone; mofarotene; molgramostim; monoclonal antibody, human chorionic gonadotrophin; monophosphoryl lipid A/myobacterium cell wall skeleton (CWS/MPL); mopidamol; multiple drug resistance gene inhibitor; multiple tumor suppressor 1-based therapy; mustard anticancer agent; mycaperoxide B; mycobacterial cell wall extract; myriaporone; N-acetyldinaline; Nsubstituted benzamides; nafarelin; nagrestip; naloxone/pentazocine combinations; napavin; naphterpin; nartograstim; nedaplatin; nemorubicin; neridronic acid; neutral endopeptidase; nilutamide; nisamycin; nitric oxide modulators; nitroxide antioxidant; nitrullyn; 06benzylguanine; octreotide; okicenone; oligonucleotides; onapristone; oracin; oral cytokine inducer; ormaplatin; osaterone; oxaliplatin; oxaunomycin; paclitaxel; paclitaxel analogues; paclitaxel derivatives; palauamine; palmitoylrhizoxin; pamidronic acid; panaxytriol; panomifene; parabactin; pazelliptine; pegaspargase; peldesine (BCX-34); pentosan polysulfate sodium; pentostatin; pentrozole; perflubron; perfosfamide; perillyl alcohol dehydrogenase; phenazinomycin; phenylacetate; phosphatase inhibitors; picibanil; pilocarpine hydrochloride; pirarubicin; piritrexim; placetin A; placetin B; plasminogen activator inhibitor; platinum complex; platinum compounds; platinum-triamine complex; porfimer sodium; porfiromycin; prednisone; propyl bis-acridone; prostaglandin J2; proteasome inhibitors; protein A-based immune modulator; protein kinase C inhibitors, microalgal; protein tyrosine phosphatase inhibitors; purine nucleoside phosphorylase inhibitors; purpurins; pyrazoloacridine; pyridoxylated hemoglobin polyoxyethylene conjugate; raf antagonists; raltitrexed; ramosetron; ras famesyl protein transferase inhibitors;
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PCT/US2013/071132 ras inhibitors; ras-GAP inhibitor; retelliptine demethylated; rhenium Re 186 etidronate; rhizoxin; ribozymes; RII retinamide; rogletimide; rohitukine; romurtide; roquinimex; rubiginone Bl; ruboxyl; safingol; saintopin; SarCNU; sarcophytol A; sargramostim; Sdi 1 mimetics; semustine; senescence derived inhibitor 1; sense oligonucleotides; signal transduction inhibitors; signal transduction modulators; single chain antigen binding protein; sizofiran; sobuzoxane; sodium borocaptate; sodium phenylacetate; solverol; somatomedin binding protein; sonermin; sparfosic acid; spicamycin D; spiromustine; splenopentin; spongistatin 1; squalamine; stem cell inhibitor; stem cell division inhibitors; stipiamide; stromelysin inhibitors; sulfinosine; superactive vasoactive intestinal peptide antagonist; suradista; suramin; swainsonine; synthetic glycosaminoglycans; tallimustine; 5-fluorouracil; leucovorin; tamoxifen methiodide; tauromustine; tazarotene; tecogalan sodium; tegafur; tellurapyrylium; telomerase inhibitors; temoporfin; temozolomide; teniposide; tetrachlorodecaoxide; tetrazomine; thaliblastine; thiocoraline; thrombopoietin; thrombopoietin mimetic; thymalfasin; thymopoietin receptor agonist; thymotrinan; thyroid stimulating hormone; tin ethyl etiopurpurin; tirapazamine; titanocene bichloride; topsentin; toremifene; totipotent stem cell factor; translation inhibitors; tretinoin; triacetyluridine; triciribine; trimetrexate; triptorelin; tropisetron; turosteride; tyrosine kinase inhibitors; tyrphostins; UBC inhibitors; ubenimex; urogenital sinus-derived growth inhibitory factor; urokinase receptor antagonists; vapreotide; variolin B; vector system, erythrocyte gene therapy; thalidomide; velaresol; veramine; verdins; verteporfin; vinorelbine; vinxaltine; volitinib; vorozole; zanoterone; zeniplatin; zilascorb; zinostatin stimalamer and the like.
In some embodiments, the additional agent used in combination with a compound of Formula (I) or a form thereof described herein is one or more immunomodulatory agent(s). Non-limiting examples of immunomodulatory agents include proteinaceous agents such as cytokines, peptide mimetics, and antibodies (e.g., human, humanized, chimeric, monoclonal, polyclonal, Fvs, ScFvs, Fab or F(ab)2 fragments or epitope binding fragments), nucleic acid molecules (e.g., antisense nucleic acid molecules and triple helices), cancer molecules, organic compounds, and inorganic compounds.
In particular, one or more immunomodulatory agents that may be used in combination with a compound of Formula (I) or a form thereof described herein include, but are not limited to, methotrexate, leflunomide, cyclophosphamide, cytoxan, cyclosporine A, minocycline, azathioprine (Imuran®), antibiotics (e.g., FK506 (tacrolimus)),
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PCT/US2013/071132 methylprednisolone (MP), corticosteroids, steroids, mycophenolate mofetil, rapamycin (sirolimus), mizoribine, deoxyspergualin, brequinar, malononitriloamindes (e.g., leflunamide), T cell receptor modulators, cytokine receptor modulators, and modulators mast cell modulators.
In one embodiment, the immunomodulatory agent is a chemotherapeutic agent. In an alternative embodiment, the immunomodulatory agent is an immunomodulatory agent other than a chemotherapeutic agent. In some embodiments, the additional agent used described herein is not an immunomodulatory agent.
In some embodiments, the additional agent that may be used in combination with a compound of Formula (I) or a form thereof described herein is one or more anti-angiogenic agent(s). Non-limiting examples of anti-angiogenic agents include proteins, polypeptides, peptides, fusion proteins, antibodies (e.g., human, humanized, chimeric, monoclonal, polyclonal, Fvs, ScFvs, Fab fragments, F(ab)2 fragments, and antigen-binding fragments thereof) such as antibodies that immunospecifically bind to TNF-α, nucleic acid molecules (e.g., antisense molecules or triple helices), organic molecules, inorganic molecules, and cancer molecules that reduce or inhibit angiogenesis. In other embodiments, the additional agent described herein is not an anti-angiogenic agent.
In some embodiments, the additional agent that may be used in combination with a compound of Formula (I) or a form thereof described herein is one or more anti-inflammatory agent(s). Νοή-limiting examples of anti-inflammatory agents include any anti-inflammatory agent useful in treating inflammatory disorders. Non-limiting examples of anti-inflammatory agents include non-steroidal anti-inflammatory drugs (NSAIDs), steroidal anti-inflammatory drugs, anticholinergics (e.g., atropine sulfate, atropine methylnitrate, and ipratropium bromide (ATROVENT®), p2-agonists (e.g., albuterol (VENTOLIN® and PROVENTIL®), bitolterol (TORNALATE®), levalbuterol (XOPONEX®), metaproterenol (ALUPENT®), pirbuterol (MAXAIR®), terbutlaine (BRETHAIRE® and BRETHINE®), albuterol (PROVENTIL®, REPETABS®, and VOLMAX®), formoterol (FORADIL AEROLIZER®), salmeterol (SEREVENT® and SEREVENT DISKUS®)), methylxanthines (e.g., theophylline (UNIPHYL®, THEO-DUR®, SLO-BID®, AND TEHO-42®)) and the like. Examples of NSAIDs include, but are not limited to, aspirin, ibuprofen, celecoxib (CELEBREX®), diclofenac (VOLTAREN®), etodolac (LODINE®), fenoprofen (NALFON®), indomethacin
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PCT/US2013/071132 (INDOCIN®), ketoralac (TORADOL®), oxaprozin (DAYPRO®), nabumentone (RELAFEN®), sulindac (CLINORIL®), tolmentin (TOLECTIN®), rofecoxib (VIOXX®), naproxen (ALEVE®, NAPROSYN®), ketoprofen (ACTRON®), nabumetone (RELAFEN®) and the like. Such NSAIDs function by inhibiting a cyclooxgenase enzyme (e.g., COX-1 and/or COX-2). Examples of steroidal anti-inflammatory drugs include, but are not limited to, glucocorticoids, dexamethasone (DECADRON®), corticosteroids (e.g., methylprednisolone (MEDROL®)), cortisone, hydrocortisone, prednisone (PREDNISONE® and DELTASONE®), prednisolone (PRELONE® and PEDIAPRED®), triamcinolone, azulfidine, inhibitors of eicosanoids (e.g., prostaglandins, thromboxanes, and leukotrienes) and the like.
In certain embodiments, the additional agent that may be used in combination with a compound of Formula (I) or a form thereof described herein is an alkylating agent, a nitrosourea, an antimetabolite, an anthracyclin, a topoisomerase II inhibitor, a mitotic inhibitor and the like. Alkylating agents include, but are not limited to, busulfan, cisplatin, carboplatin, cholormbucil, cyclophosphamide, ifosfamide, decarbazine, mechlorethamine, mephalen, themozolomide and the like. Nitrosoureas include, but are not limited to carmustine (BiCNU®), lomustine (CeeNU®) and the like. Antimetabolites include, but are not limited to, 5-fluorouracil, capecitabine, methotrexate, gemcitabine, cytarabine, fludarabine and the like. Anthracyclins include but are not limited to daunorubicin, doxorubicin, epirubicin, idarubicin, mitoxantrone and the like. Topoisomerase II inhibitors include, but are not limited to, topotecan, irinotecan, etopiside (VP-16), teniposide and the like. Mitotic inhibitors include, but are not limited to taxanes (paclitaxel, docetaxel), and the vinca alkaloids (vinblastine, vincristine, and vinorelbine) and the like.
In more specific embodiments, the additional anti-cancer agent, anti-proliferative agent or chemotherapeutic agent that may be used in combination with a compound of Formula (I) or a form thereof described herein includes, and is not limited to aflibercept, amsacrine, bleomycin, busulfan, capecitabine, carboplatin, carmustine, chlorambucil, cisplatin, cladribine, clofarabine, crisantaspase, cyclophosphamide, cytarabine, dacarbazine, dactinomycin, daunorubicin (IV and liposomal), docetaxel, doxorubicin (IV and liposomal), enzastaurin, epirubicin, etoposide, fludarabine, 5-fluorouracil (5-FU), gemcitabine, gliadel implants, hydroxycarbamide, idarubicin, ifosfamide, imatinib mesylate, irinotecan, lanreotide, lenalidomide, leucovorin, lomustine, melphalan, mercaptopurine, mesna,
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PCT/US2013/071132 methotrexate, mitomycin, mitoxantrone, octreotide, oxaliplatin, paclitaxel, pemetrexed, pentostatin, procarbazine, raltitrexed, satraplatin, sorafenib, streptozocin, sunitinib, tegafur-uracil, temozolomide, teniposide, thalidomide, thiotepa, tioguanine, topotecan, treosulfan, vatalanib, vinblastine, vincristine, vindesine, vinorelbine, volitinib, ZD6474, monoclonal antibodies (such as bevacizumab, cetuximab, IMC-A12, IMC-1121B, medi-522, rituximab and the like), hormonal agents (such as anastrozole, bicalutamide, buserelin, cyproterone, diethylstilbestrol, exemestane, flutamide, goserelin (breast and prostrate), letrozole, leuprorelin, medroxyprogesterone, megestrol acetate, tamoxifen, toremifene, triptorelin and the like), biological agents (such as interferon, interleukin-12 and the like), angiogenesis receptor tyrosine kinase (RTK) inhibitors (such as AE-941, angiostatin, carboxyamidotriazole, cilengitide, endostatin, halofuginone hydrobromide, 2-methoxyestradiol, squalamine lactate, SU6668 and the like), tubulin binding agents (such as combretastatin A4 phosphate and the like), matrix metalloproteinase inhibitors (such as BMS-275291 and the like) and/or serine/threonine/tyrosine kinase inhibitors and an optional nonsteroidal or COX-2 anti-inflammatory agents (such as celecoxib and the like) or corticosteroid (such as prednisone and the like).
In more particular embodiments, one or more additional anti-cancer, anti-proliferative or chemotherapeutic agents that may be used in combination with a compound of Formula (I) or a form thereof described herein is selected from bevacizumab, carboplatin, cisplatin, docetaxel, doxorubicin, exemestane, gemcitabine, 5-fluorouracil, imatinib, irinotecan, sorafenib, sunitinib, temozolomide, volitinib or combinations thereof.
In some embodiments, a compound of Formula (I) or a form thereof described herein and one or more additional anti-cancer, anti-proliferative or chemotherapeutic agents is used in combination with radiation therapy comprising the use of x-rays, gamma rays and other sources of radiation to destroy cancer cells or tumor cells. In specific embodiments, the radiation therapy is administered as external beam radiation or teletherapy, wherein the radiation is directed from a remote source. In other embodiments, the radiation therapy is administered as internal therapy or brachytherapy wherein a radioactive source is placed close to cancer cells, tumor cells and/or a tumor mass.
Currently available anti-cancer, anti-proliferative or chemotherapeutic agents, their dosage regimens, routes of administration and recommended usage alone or in combination
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PCT/US2013/071132 are known in the art and have been described in literature such as the Physician’s Desk Reference.
Any anti-cancer, anti-proliferative or chemotherapeutic agent or anti-cancer therapy which is known to be useful, or which has been used or is currently being used for the treatment of a cancer mediated by Bmi-1, can be used in combination with compounds of Formula (I) or a form thereof described herein. See, e.g., Gilman et al., Goodman and Gilman’s: The Pharmacological Basis of Therapeutics, 10th ed., McGraw-Hill, New York, 2001; The Merck Manual of Diagnosis and Therapy, Berkow, M.D. et al. (eds.), 17th Ed., Merck Sharp & Dohme Research Laboratories, Rahway, NJ, 1999; Cecil Textbook of Medicine, 20th Ed., Bennett and Plum (eds.), W.B. Saunders, Philadelphia, 1996, and Physician’s Desk Reference for information regarding cancer therapies (e.g., using prophylactic or therapeutic agents) which have been or are currently being used for preventing, treating and/or managing a cancer mediated by Bmi-1.
Pharmaceutical Compositions
The present description is also directed to a pharmaceutical composition comprising an effective amount of a compound of Formula (I) or a form thereof in admixture with a pharmaceutically acceptable excipient.
An embodiment described herein includes a pharmaceutical composition made by the process of admixing a compound of Formula (I) or a form thereof with a pharmaceutically acceptable excipient. The pharmaceutical composition may also be formulated to achieve a physiologically compatible pH of about pH 7, ranging from about pH 3 to about pH 11.
Another embodiment of the present includes the use of a compound of Formula (I) or a form thereof in a pharmaceutical composition for use in treating a cancer mediated by Bmi-1 comprising an effective amount of a compound of Formula (I) or a form thereof in admixture with a pharmaceutically acceptable excipient.
As used herein, the term “composition” means a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combination of the specified ingredients in the specified amounts.
In another embodiment, the pharmaceutical composition may comprise a combination product of one or more compounds of Formula (I) or a form thereof described herein and one
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PCT/US2013/07U32 or more additional agents useful in the treatment of a cancer mediated by Bmi-1, such as an anti-cancer, anti-proliferative, chemotherapeutic or biochemotherapeutic agent.
The term “pharmaceutically acceptable excipient” refers to a pharmacologically inactive substance formulated for administration with an active pharmaceutical agent, such as the compounds of Formula (I) or a form thereof described herein. The term refers to any pharmaceutical excipient that may be administered without undue toxicity. Pharmaceutically acceptable excipients may be determined in part by the particular composition being administered, as well as by the particular mode of administration and/or dosage form. Nonlimiting examples of pharmaceutically acceptable excipients include carriers, solvents, stabilizers, adjuvants, diluents, etc. Accordingly, there exists a wide variety of suitable formulations of pharmaceutical compositions as described herein (see, e.g., Remington’s Pharmaceutical Sciences).
Suitable excipients may be carrier molecules that include large, slowly metabolized macromolecules such as proteins, polysaccharides, polylactic acids, polyglycolic acids, polymeric amino acids, amino acid copolymers, and inactive virus particles. Other exemplary excipients include antioxidants such as ascorbic acid; chelating agents such as EDTA; carbohydrates such as dextrin, hydroxyalkylcellulose, hydroxyalkylmethylcellulose, stearic acid; liquids such as oils, water, saline, glycerol and ethanol; wetting or emulsifying agents; pH buffering substances; and the like. Liposomes are also included within the definition of pharmaceutically acceptable excipients.
The pharmaceutical compositions described herein may be formulated in any form suitable for the intended method of administration. Suitable formulations for oral administration include solids, liquid solutions, emulsions and suspensions, while suitable inhaleable formulations for pulmonary administration include liquids and powders. Alternative formulations include syrups, creams, ointments, tablets, and lyophilized solids which can be reconstituted with a physiologically compatible solvent prior to administration.
When intended for oral use for example, tablets, troches, lozenges, aqueous or oil suspensions, non-aqueous solutions, dispersible powders or granules (including micronized particles or nanoparticles), emulsions, hard or soft capsules, syrups or elixirs may be prepared. Compositions intended for oral use may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions, and such compositions
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PCT/US2013/071132 may contain one or more agents including sweetening agents, flavoring agents, coloring agents and preserving agents, in order to provide a palatable preparation.
Pharmaceutically acceptable excipients suitable for use in conjunction with tablets include, for example, inert fillers, such as celluloses, calcium or sodium carbonate, lactose, calcium or sodium phosphate; disintegrating agents, such as croscarmellose sodium, crosslinked povidone, maize starch, or alginic acid; binding agents, such as povidone, starch, gelatin or acacia; and lubricating agents, such as magnesium stearate, stearic acid or talc. Tablets may be uncoated or may be coated by known techniques including microencapsulation to delay disintegration and adsorption in the gastrointestinal tract and thereby provide a sustained action over a longer period.
Formulations for oral use may be also presented as hard gelatin capsules where the active ingredient is mixed with an inert solid diluent, for example celluloses, lactose, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with non-aqueous or oil medium, such as glycerin, propylene glycol, polyethylene glycol, peanut oil, liquid paraffin or olive oil.
In other embodiments, pharmaceutical compositions described herein may be formulated as suspensions comprising a compound of Formula (I) or a form thereof described herein in admixture with at least one pharmaceutically acceptable excipient suitable for the manufacture of a suspension. In yet other embodiments, pharmaceutical compositions described herein may be formulated as dispersible powders and granules suitable for preparation of a suspension by the addition of one or more excipient(s).
Excipients suitable for use in connection with suspensions include suspending agents, such as sodium carboxymethyl cellulose, methylcellulose, hydroxypropyl methylcelluose, sodium alginate, polyvinylpyrrolidone, gum tragacanth, gum acacia, dispersing or wetting agents such as a naturally occurring phosphatide (e.g., lecithin), a condensation product of an alkylene oxide with a fatty acid (e.g., polyoxyethylene stearate), a condensation product of ethylene oxide with a long chain aliphatic alcohol (e.g., heptadecaethyleneoxycethanol), a condensation product of ethylene oxide with a partial ester derived from a fatty acid and a hexitol anhydride (e.g., polyoxyethylene sorbitan monooleate); and thickening agents, such as carbomer, beeswax, hard paraffin or cetyl alcohol. The suspensions may also contain one or more preservatives such as acetic acid, methyl and/or n-propyl p-hydroxy-benzoate; one or
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PCT/US2013/071132 more coloring agents; one or more flavoring agents; and one or more sweetening agents such as sucrose or saccharin.
The pharmaceutical compositions described herein may also be in the form of oil-inwater emulsions. The oily phase may be a vegetable oil, such as olive oil or arachis oil, a mineral oil, such as liquid paraffin, or a mixture of these. Suitable emulsifying agents include naturally-occurring gums, such as gum acacia and gum tragacanth; naturally occurring phosphatides, such as soybean lecithin, esters or partial esters derived from fatty acids; hexitol anhydrides, such as sorbitan monooleate; and condensation products of these partial esters with ethylene oxide, such as polyoxyethylene sorbitan monooleate. The emulsion may also contain sweetening and flavoring agents. Syrups and elixirs may be formulated with sweetening agents, such as glycerol, sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative, a flavoring or a coloring agent.
Additionally, the pharmaceutical compositions described herein may be in the form of a sterile injectable preparation, such as a sterile injectable aqueous emulsion or oleaginous suspension. Such emulsion or suspension may be formulated according to the known art using those suitable dispersing or wetting agents and suspending agents which have been mentioned above. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, such as a solution in 1,2-propane-diol. The sterile injectable preparation may also be prepared as a lyophilized powder. Among the acceptable Vehicles and solvents that may be employed are water, Ringer’s solution, isotonic sodium chloride solution and the like. In addition, sterile fixed oils may be employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic mono- or di-glycerides. In addition, fatty acids such as oleic acid may likewise be used in the preparation of injectables.
The compounds of Formula (I) or a form thereof described herein may be substantially modified by substitutions or additions of chemical or biochemical moieties which make them more suitable for delivery (e.g., increase solubility, bioactivity, palatability, decrease adverse reactions, etc.), for example by esterification, glycosylation, PEGylation and the like.
In some embodiments, the compound of Formula (I) or a form thereof described herein is formulated for oral administration in formulations that enhance the oral
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PCT/US2013/071132 bioavailability of such compounds of Formula (I) or a form thereof. As such, pharmaceutical compositions described herein may comprise a effective amount of a compound of Formula (I) or a form thereof, together with at least one pharmaceutically acceptable excipient selected from medium chain fatty acids or propylene glycol esters thereof (e.g., propylene glycol esters of edible fatty acids such as caprylic and capric fatty acids) and pharmaceutically acceptable surfactants, such as polyoxyl 40 hydrogenated castor oil and the like.
In other embodiments, the bioavailability of a compound of Formula (I) or a form thereof may be enhanced by using particle size optimization techniques including, but not limited to, the preparation of nanoparticles or nanosuspensions using techniques known to those skilled in art. The compound forms present in such preparations include amorphous, partially amorphous, partially crystalline or crystalline forms.
In alternative embodiments, the pharmaceutical composition may further comprise one or more aqueous solubility enhancer(s), such as a cyclodextrin. Nonlimiting examples of cyclodextrin include hydroxypropyl, hydroxyethyl, glucosyl, maltosyl and maltotriosyl derivatives of α-, β-, and γ-cyclodextrin, and hydroxypropyl^-cyclodextrin (HPBC). In some embodiments, the pharmaceutical composition further comprises HPBC in a range of from about 0.1% to about 20%, from about 1% to about 15%, or from about 2.5% to about 10%. The amount of solubility enhancer employed may depend on the amount of the active pharmaceutical ingredient in the composition.
General Synthetic Examples
As disclosed herein, the methods for preparing the compounds of Formula (I) or a form thereof described herein commonly use standard, well-known synthetic methodology. Many of the starting materials are commercially available or can be prepared in the Specific Synthetic Examples that follow using techniques known to those skilled in the art. Functional transformations to modify substituents may also be undertaken where chemically feasible and are considered to be included within the scope of the General Schemes and the knowledge of a person of ordinary skill in the art. Compounds of Formula (I) or a form thereof can be prepared as described in the Schemes below.
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Scheme A Benzimidazole Substituted Pyrimidine Compounds
Ra Ra
Figure AU2013348009C1_D0109
Figure AU2013348009C1_D0110
An amine substituted Compound Al (wherein Xi represents a halogen atom selected from bromo, chloro or iodo) is coupled with various substituted aryl, heteroaryl or heterocyclyl amines (wherein PG represents an optionally present protecting group monosubstituted on the amine) in the presence of a strong base (such as KOtBu, NaOtBu, NaC/Ain, NaH, NaHMDS and the like) in a solvent (such as THF, DMF and the like) to provide a Compound A2.
When one or both of R2 and R3 are optionally halogen, the product Compound A2 is obtained as a mixture of regioisomers, wherein the term “Sep” refers to isolating the desired Compound A2 isomer to be carried forward from the mixture using separation techniques known to those of ordinary skill in the art, followed by deprotection.
Alternatively, Compound A2 may be prepared by reacting Compound Al with various substituted aryl, heteroaryl or heterocyclyl amines (wherein the protecting group is absent) in the presence of a mixture of a phosphino ligand:palladium source (wherein the palladium source is selected from Pd2(dba).3, PdCl2(allyl), PdCl2(ACN), [Pd(OAc)2]3 and the like and the phosphino ligand is selected from PCy3, Q-Phos, XPhos and the like; alternatively, a commercially available catalyst such as Pd(dppf)Cl2, Pd(PPhs)4 and the like may be used), followed by separation as needed.
Compound A3 may be prepared by reacting Compound A2 with a substituted ortho-halo-nitro benzene (wherein Xi represents a halogen atom selected from bromo, chloro or iodo) in the presence of a transition metal catalyst (such as a catalyst containing a metal selected from copper, palladium and the like).
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Alternatively, Compound A3 may be prepared by reacting Compound A2 with the substituted ortho-halo-nitro benzene (wherein X2 represents a halogen atom selected from bromo, chloro, fluoro or iodo) in the presence of a strong base (such as KOtBu, NaOtBu, NaOlAm, NaH, NaHMDS and the like) in a solvent (such as THF, DMF and the like).
Compound A4 is prepared by reacting Compound A3 in the presence of hydrogen and a catalyst (such as nickel, platinum, palladium on carbon and the like).
Compound A6 is prepared by condensation of Compound A4 with an orthoester Compound A5 (wherein Rb represents an additional optional R5 substituent and Rc represents C]_3alkyl). Compound A6 may also be prepared by cyclizing Compound A4 with a variety of reactants to obtain the addition of the optional R5 substituent. For example, the reactant may be TCDI, wherein the additional optional R5 substituent is a thio-carbonyl which may be further substituted.
Figure AU2013348009C1_D0111
Figure AU2013348009C1_D0112
Alternatively, Compound A3 is prepared by cross-coupling of Compound A7 (wherein Xi represents a halogen atom selected from bromo, chloro or iodo) with a nitro substituted amine Compound A8 (wherein Ar represents an aromatic or heteroaromatic ring; and, wherein Ra represents one, two or three optional R5 substituents) via a palladium catalyzed cross-coupling reaction using a mixture of a phosphino ligand .-palladium source (wherein the palladium source is selected from Pd2(dba)3, PdCl2(allyl), PdCl2(ACN), [Pd(OAc)2]3 and the like and the phosphino ligand is selected from PCy3, Q-Phos, XPhos and the like; alternatively, a commercially available catalyst such as Pd(dppf)Cl2, Pd(PPh3)4 and the like may be used).
When one or both of R2 and R3 are optionally halogen, the product Compound A3 is obtained as a mixture of regioisomers, wherein the term “Sep” refers to isolating the desired Compound A3 isomer to be carried forward from the mixture using separation techniques known to those of ordinary skill in the art.
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Scheme B Imidazof l,2-a]pyridine Substituted Pyrimidine Compounds
Figure AU2013348009C1_D0113
Figure AU2013348009C1_D0114
Compound Bl is prepared by condensation of a substituted 2-amino-pyridine (wherein Ra represents represents one, two or three optional R5 substituents) with an ahalogenated ketoester (wherein Rb represents an additional optional R5 substituent and Re represents Ci_3alkyl).
Compound B2 is prepared by treating Compound Bl with an ammonia source (such as NH4CI, NH3 and the like) in the presence of an organoaluminum reagent (such AlMe3 in toluene and the like).
Compound B3 (wherein X| represents a halogen atom selected from bromo, chloro or iodo) is prepared by condensation of Compound B2 with a substituted alkyl ester (such as a β-keto ester or a substituted acrylate in a solvent such as phenyl ether and the like; wherein X3 represents a leaving group such as C 1.3 alkoxy, benzoxy or halogen) followed by reflux in the presence of a halogenation reagent (such as POCI3, POBr3 and the like).
Compound B4 is prepared by coupling Compound B3 with various substituted aryl, heteroaryl or heterocyclyl amines (wherein PG represents an optionally present protecting group monosubstituted on the amine) in the presence of a strong base (such as KOtBu, NaOtBu, NaO‘Am, NaH, NaHMDS and the like) in a solvent (such as THF, DMF and the like).
Alternatively, Compound B4 may be prepared by reacting Compound B3 with a substituted aryl, heteroaryl or heterocyclyl amine (wherein the protecting group is absent) via
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PCT/US2013/071132 a palladium catalyzed cross-coupling reaction using a mixture of a phosphino ligandrpalladium source (wherein the palladium source is selected from Pd2(dba)3, PdC12(allyl), PdC12(ACN), [Pd(OAc)2]3 and the like and the phosphino ligand is selected from PCy3, Q-Phos, XPhos and the like; alternatively, a commercially available catalyst such as Pd(dppf)C12, Pd(PPh3)4 and the like may be used).
Scheme C 4,6-Diamino Substituted Pyrimidine Compounds
Figure AU2013348009C1_D0115
Figure AU2013348009C1_D0116
C2 C3
Compound Cl is prepared by condensation of a substituted 2-amino-pyridine (wherein Ra represents represents one, two or three optional R5 substituents) and an α-halogenated ketone (wherein X4 represents a leaving group such as chloro or bromo and Rb represents an additional optional R5 substituent) at reflux in an organic solvent (such as acetonitrile and the like).
Compound C2 is prepared by reacting Compound Cl with a substituted pyrimidine compound (wherein Xj represents a halogen atom selected from bromo, chloro or iodo) via a palladium catalyzed cross-coupling reaction using a mixture of a phosphino ligand:palladium source (wherein the palladium source is selected from Pd2(dba)3, PdC12(allyl), PdC12(ACN), [Pd(OAc)2]3 and the like and the phosphino ligand is selected from PCy3, Q-Phos, XPhos and the like; alternatively, a commercially available catalyst such as Pd(dppf)C12, Pd(PPh3)4 and the like may be used) and at least 2 equivalents of a base (such as cesium acetate and the like) in an organic solvent (such as dimethylacetamide and the like), undergoing Heck coupling. The reaction may be carried out at elevated temperatures up to 100°C.
Compound C3 is prepared by treating Compound C2 with a deprotection reagent (such as 20-40% TFA in DCM and the like) at ambient or elevated temperature.
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Scheme D 4,6-Diamino Substituted Pyrimidine Compounds
Figure AU2013348009C1_D0117
Figure AU2013348009C1_D0118
Figure AU2013348009C1_D0119
Figure AU2013348009C1_D0120
Figure AU2013348009C1_D0121
Figure AU2013348009C1_D0122
Figure AU2013348009C1_D0123
Compound DI is prepared by a condensation reaction with a substituted malonate compound and an amidated Ri group in solution with a sodium alkoxide-solvent mixture (such as NaOMe in MeOH or NaOEt in EtOH and the like).
Compound D2 (wherein Xi represents a halogen atom selected from bromo, chloro or iodo) is prepared by refluxing Compound DI in the presence of a halogenation reagent (such as POCI3, POBr3 and the like).
Compound D3 is prepared by mono-amination of Compound D2 with various substituted aryl, heteroaryl or heterocyclyl amines in a solvent (wherein the solvent is selected from EtOH, THF, DMF, mixtures thereof and the like).
Compound D4 is prepared by treating Compound D3 with an aqueous ammonia source in a mixture with a solvent (wherein the solvent is selected from CH3CN, DMSO, 15 mixtures thereof and the like).
Scheme E Benzimidazole Substituted Pyrimidine Compounds
Figure AU2013348009C1_D0124
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Figure AU2013348009C1_D0125
Figure AU2013348009C1_D0126
A 2-methylsulfonyl substituted Compound E2 is prepared by reacting a 2-methylthio substituted pyrimidine Compound El (wherein Xi represents a halogen atom selected from bromo, chloro or iodo and Re represents Cj^alkyl) with an oxidizing agent (such as mCPBA, MPS and the like) in a solvent (such as CH2CI2 and the like) at a suitable temperature.
Compound E4 is prepared by reacting Compound E2 with a nitro substituted amine Compound E3 (wherein Ar represents an aromatic or heteroaromatic ring; and, wherein Ra represents one, two or three optional R5 substituents) in the presence of a strong base (such as KOtBu, NaOtBu, NaOlAm, NaH, NaHMDS and the like) in a solvent (such as THF, DMF and the like). The amine substituent on Compound E3 may be optionally monosubstituted on the amine with a protecting group.
Compound E5 is prepared by reacting Compound E4 in the presence of hydrogen and a catalyst (such as nickel, platinum, palladium on carbon and the like).
Compound E6 is prepared by condensation of Compound E5 with an orthoester Compound A5 (wherein Rb represents an additional optional R5 substituent and Rc represents Ci-3alkyl). Compound E6 may also be prepared by cyclizing Compound E5 with a variety of reactants to obtain the addition of an optional R5 substituent. For example, the reactant may be TCDI, wherein the additional optional R5 substituent is a thio-carbonyl which may be further substituted.
Compound E7 may be prepared by reacting Compound E6 with various substituted aryl, heteroaryl or heterocyclyl amines in a solvent (wherein the solvent is selected from EtOH, THF, DMF, mixtures thereof and the like).
When R3 is optionally halogen, the product Compound E7 is obtained as a mixture of regioisomers, wherein the term “Sep” refers to isolating the desired Compound E7 isomer to be carried forward from the mixture using separation techniques known to those of ordinary skill in the art, followed by deprotection.
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Figure AU2013348009C1_D0127
nh2
NHC(O)H
Sep
Figure AU2013348009C1_D0128
Alternatively, Compound E7 may be prepared by reacting Compound E6 with a substituted aryl, heteroaryl or heterocyclyl amine or amide (wherein the protecting group is absent) via a palladium catalyzed cross-coupling reaction using a mixture of a phosphino 5 ligand:palladium source (wherein the palladium source is selected from Pd2(dba)3, PdCl2(allyl), PdCl2(ACN), [Pd(OAc)2]3 and the like and the phosphino ligand is selected from PCy3, Q-Phos, XPhos and the like; alternatively, a commercially available catalyst such as Pd(dppf)Cl2, Pd(PPh3)4 and the like may be used).
R2 R2
Figure AU2013348009C1_D0129
Compound E9 may be prepared directly by reacting Compound E2 with a Compound
E8 (such as an Rj substituent having an acidic proton group, wherein X5 represents a reactive hydrogen atom) in the presence of a strong base (such as KOtBu, NaOtBu, NaOlAm, NaH, NaHMDS and the like). Compound E9 may be carried forward in place to Compound E6 to provide a Compound of Formula (I).
Scheme F Substituted Pyrimidine Compounds
Figure AU2013348009C1_D0130
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Compound Fl is prepared by reacting Compound El (wherein X] represents a halogen atom selected from bromo, chloro or iodo and Re represents Ci^alkyl) with a substituted aryl, heteroaryl or heterocyclyl amine (wherein PG represents an optionally present protecting group monosubstituted on the amine) in the presence of a strong base (such as KOtBu, NaOtBu, NaO‘Am, NaH, NaHMDS and the like) in a solvent (such as THF, DMF and the like) at a suitable temperature.
When R3 is optionally halogen, the product Compound Fl is obtained as a mixture of regioisomers, wherein the term “Sep” refers to isolating the desired Compound Fl isomer to be carried forward from the mixture using separation techniques known to those of ordinary skill in the art.
Alternatively, Compound Fl is prepared by reacting Compound El with a substituted aryl, heteroaryl or heterocyclyl amine or amide (wherein the protecting group is absent) via a palladium catalyzed cross-coupling reaction using a mixture of a phosphino ligand:palladium source (wherein the palladium source is selected from Pd2(dba)3, PdC12(allyl), PdCl2(ACN), [Pd(OAc)2]3 and the like and the phosphino ligand is selected from PCy3, Q-Phos, XPhos and the like; alternatively, a commercially available catalyst such as Pd(dppf)Cl2, Pd(PPh3)4 and the like may be used).
Compound F2 is prepared by reacting Compound Fl with an oxidizing agent (such as mCPBA, MPS and the like) in a solvent (such as CH2CI2 and the like).
Compound F2 may be reacted with a Compound E8 (such as an Ri substituent having an acidic proton group, wherein X5 represents a reactive hydrogen atom) in the presence of a strong base (such as KOtBu, NaOtBu, NaO'Am, NaH, NaHMDS and the like) to provide a Compound F3, representative of a Compound of Formula (I).
When R2 is halogen, Compound F3 may be treated with a substituted amine in a mixture with a solvent (wherein the solvent is selected from CH3CN, DMSO, mixtures thereof and the like) to provide a Compound F4, representative of a Compound of Formula (ΠΙ).
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Scheme G Oxide Substituted Pyrimidine Compounds
Figure AU2013348009C1_D0131
Compound G1 may be reacted with an oxidizing agent (such as mCPBA, MPS and the like) to provide a Compound G2, representative of a Compound of Formula (IV).
Scheme H Substituted Pyrimidine Compounds
Figure AU2013348009C1_D0132
A Compound H3 is prepared by reacting a Compound Hl (wherein Xi represents a halogen atom selected from bromo, chloro or iodo) with a Compound H2 (wherein Ri is a substituted heteroaromatic or heterocyclic monocyclic or bicyclic ring system and X& represents a reactive group such as a boronic acid, boronate ester, trialkyltin, zinc chloride and the like attached to a carbon atom of Rj), in the presence of a mixture of a phosphino ligand:palladium source (wherein the palladium source is selected from Pd2(dba)3, PdCl2(allyl), PdC12(ACN), [Pd(OAc)2]3 and the like and the phosphino ligand is selected from PCy3, Q-Phos, XPhos and the like; alternatively, a commercially available catalyst such as Pd(dppf)Cl2, Pd(PPh3)4 and the like may be used).
When one or both of R2 and R3 are optionally halogen, the product Compound H3 may be obtained as a mixture of regioisomers, wherein the term “Sep” refers to isolating the desired Compound H3 isomer to be earned forward from the mixture using separation techniques known to those of ordinary skill in the art.
Compound F3 is prepared by reacting Compound H3 with various substituted aryl, heteroaryl or heterocyclyl amines in a solvent (wherein PG represents an optionally present protecting group monosubstituted on the amine; and, wherein the solvent is selected from EtOH, THF, DMF, mixtures thereof and the like), followed by separation and deprotection as needed.
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R2
Figure AU2013348009C1_D0133
H3 Rx rx NH2 or NHC(O)H
Sep
Figure AU2013348009C1_D0134
Alternatively, Compound F3 is prepared by reacting a Compound H3 with various substituted aryl, heteroaryl or heterocyclyl amines or amides in the presence of a mixture of a phosphino ligand.-palladium source (wherein the palladium source is selected from Pd2(dba)3, 5 PdC12(allyl), PdCl2(ACN), [Pd(OAc)2]3 and the like and the phosphino ligand is selected from PCy3, Q-Phos, XPhos and the like; alternatively, a commercially available catalyst such as Pd(dppf)Cl2, Pd(PPh3)4 and the like may be used). When a Compound H3 is reacted with an amide, the resulting intermediate product is hydrolyzed under basic conditions with a reagent (such as NaOH, KOH, Li OH and the like) at a suitable temperature, followed by separation as needed to obtain product Compound F3.
R2
Figure AU2013348009C1_D0135
H1
Figure AU2013348009C1_D0136
Alternatively, Compound H3 may be prepared via a Heck reaction of Compound Hl with Compound E8, followed by separation as needed.
R2
Figure AU2013348009C1_D0137
R4 H7
Figure AU2013348009C1_D0138
Alternatively, Compound F3 is prepared by reacting Compound H7 with a substituted
Compound H2 (wherein R i is a substituted hetero aromatic or heterocyclic monocyclic or bicyclic ring system and Χή represents a reactive group such as a boronic acid, boronate ester, trialkyltin, zinc chloride and the like attached to a carbon atom of Rj).
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Figure AU2013348009C1_D0139
Figure AU2013348009C1_D0140
Figure AU2013348009C1_D0141
Alternatively, Compound F3 may be prepared via a Heck reaction of Compound H7 with Compound E8 (wherein X5 represents a reactive hydrogen group), followed by separation as needed.
Scheme I Substituted Pyrimidine Compounds
R2
Figure AU2013348009C1_D0142
Figure AU2013348009C1_D0143
Compound F3 is prepared by reacting a substituted Compound II with a Compound 12 (such as various substituted aryl, heteroaryl or heterocyclyl ring systems, wherein X] represents a halogen atom selected from bromo, chloro or iodo) in the presence of a transition metal catalyst (such as a catalyst containing a metal selected from copper, palladium and the like).
Figure AU2013348009C1_D0144
Figure AU2013348009C1_D0145
Compound F3 is prepared by reacting a substituted Compound II with a Compound 13 (such as various substituted aryl, heteroaryl or heterocyclyl ring systems, wherein X7 represents a ketone or aldehyde leaving group) in the presence of a borohydride (such as NaCNBH3 or NaBH(OAc)3 and the like).
Specific Synthetic Examples
To assist in understanding the scope of the compounds of Formula (I) or a form thereof described herein, the following Specific Examples are included. The experiments relating to the compounds of Formula (I) or a form thereof described herein should not, of course, be construed as specifically limiting the scope of the compounds of Formula (I) or a 108
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Other than in the working examples, unless indicated to the contrary, all numbers expressing quantities of ingredients, reaction conditions, experimental data, and so forth used in the specification and claims are to be understood as being modified by the term “about”. Accordingly, all such numbers represent approximations that may vary depending upon the desired properties sought to be obtained by a reaction or as a result of variable experimental conditions. Therefore, within an expected range of experimental reproducibility, the term “about” in the context of the resulting data, refers to a range for data provided that may vary according to a standard deviation from the mean. As well, for experimental results provided, the resulting data may be rounded up or down to present data consistently, without loss of significant figures. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should be construed in light of the number of significant digits and ordinary rounding techniques.
While the numerical ranges and parameters setting forth the characterization of the compounds of Formula (I) or a form thereof described herein are approximations, the numerical values set forth in the working examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements.
The compounds of Formula (I) or a form thereof provided herein are described in more detail with reference to the following non-limiting examples, which are offered to more fully illustrate the scope of the compounds of Formula (I) or a fonn thereof described herein, but are not to be construed as limiting the scope thereof. The examples illustrate the preparation of compounds of Formula (I) or a form thereof described herein, and the testing of these compounds of Formula (I) or a fonn thereof in vitro and/or in vivo. Those of skill in the art will understand that the synthesis techniques described in these examples represent techniques that fall within the practice of those having ordinary skill in the chemical arts, and as such constitute preferred modes for the practice thereof. However, it should be appreciated that those having skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific methods that are disclosed herein
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The reagents and solvents were used as purchased (from a variety of vendors), except where noted. Where applicable, the term “Celite” is used as shown in the following examples to represent the tradename CELITE® (brand of diatomaceous earth). Where applicable, chromatographic separations were performed using techniques and equipment commonly available such as, for example, by using an ISCO CombiFlash® Rf system. Where applicable, NMR spectra were obtained using techniques and equipment commonly available such as, for example, by using a Bruker Avance III500 spectrometer with deuterated solvents such as, for example, DMSO-tA or residual solvent as standard. Where applicable, melting points were determined using techniques and equipment commonly available such as, for example, by using a SRS OptiMelt® MPA 100 (values as obtained without correction/calibration). Where applicable, TLC analysis was performed using techniques and equipment commonly available such as, for example, by using Aldrich 254 nm glass-backed plates (60 A, 250 pm), visualized using UV and I2 stains. Where applicable, ESI mass spectra were obtained using techniques and equipment commonly available such as, for example, by using an ACQUITY UPLC® System, with values shown as [M+H]+ or [M-H]', unless otherwise indicated. Where applicable, the structure of the product was obtained via a 2D NOESY (Nuclear Overhauser SpectroscopY) experiment.
The following abbreviations are provided to ensure the terms used herein are unambiguous to one skilled in the art:
Abbreviation Meaning
AcOH or HOAc acetic acid
ACN or MeCN acetonitrile
AlMe3 trimethylaluminum
APC allylpalladium (II) chloride dimer
Boe tert-butoxycarbonyl
CsOAc cesium acetate
DCM or CH2C12 dichloromethane
DME dimethyl ether
DMF dimethyl formamide
DMA dimethylacetamide
DMAP 4-dimethylaminopyridine
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Abbreviation Meaning
DMSO EtOAc EtOH HPLC h, hr, min, s iPrMgCl*LiCl iPrOAc K2CO3 K3PO4 KOtBu or t-BuOK LC/MS, LCMS or LC-MS MeOH MeNH2 x HC1 MS dimethylsulfoxide ethyl acetate ethanol high performance liquid chromatography hour (h or hr), minute (min), second (s) isopropylmagnesium chloride lithium chloride complex isopropyl acetate potassium carbonate potassium phosphate potassium ZerZ-butoxide liquid chromatographic mass spectroscopy methanol methanamine hydrochloride mass spectroscopy
m.p. MPS NaH NaHCO3 NaHMDS NaIO4 NaOH NaOtAm NaOMe NaOEt NaOtBu NCS NH4CI NH4OH NIS NMP NMR Oxone PC15 PCy3 [Pd] Pd/C° melting point (shown in °Centigrade) potassium peroxymonosulfate (2KHSOs-KHSO4-K2SO4) sodium hydride sodium bicarbonate sodium hexamethyldisilazide sodium periodate sodium hydroxide sodium ZerZ-pentoxide sodium methoxide sodium ethoxide sodium Ze/7-butoxide N-chlorosuceinimide ammonium chloride ammonium hydroxide N-iodosuccinimide N-methylpyrrolidone nuclear magnetic resonance potassium peroxymonosulfate phosphorus perchloride or phosphorus pentachloride tricyclohexylphosphine palladium palladium on carbon 111
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Abbreviation Meaning
Pd2(dba)3 or Pd2dba3 Pd(dppf)Cl2 PdCl2(ACN) . PdCl2(allyl) [Pd(OAc)2]3 Pd(PPh3)4 POCI3 PPh3 psi Pt/C PTSA Q-Phos or QPhos RT TBSO or OTBS TCDI t-Bu TEA, NEt3, Et3N TFA TFAA THF TsOH X H2O UPLC Xphos or XPhos tris(dibenzylideneacetone)dipalladium(0) [1,1 '-bis(diphenylphosphino)ferrocene] dichloropalladium(II) bis(acetonitrile)dichloropalladium(II) chloroallylpalladium(II) dimer palladium (II) acetate tetrakis(triphenylphosphine)palladium phosphorus oxychloride triphenylphosphine pounds per square inch pressure platinum on carbon p-toluenesulfonic acid 1,2,3,4,5-pentaphenyl-l '-(di-tert-butylphosphino)ferrocene room temperature Zeri-butyldimethylsilyloxy 1,1’ -thiocarbonyldiimidazole tert-butyl triethylamine trifluoroacetic acid trifluoroacetic anhydride tetrahydro furan p-toluenesulfonic acid monohydrate Ultra Performance Liquid Chromatography 2-dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl
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Example 1
N-(l,3-benzodioxol-5-yl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-
Figure AU2013348009C1_D0146
NH4CI
ΜΘ3ΑΙ
Figure AU2013348009C1_D0147
Figure AU2013348009C1_D0148
Figure AU2013348009C1_D0149
Figure AU2013348009C1_D0150
Step 1. To a solution of ethyl 4,4,4-trifluoro-3-oxobutanoate (9.0 g, 48.9 mmol) in CH2CI2 (50 mL) was added bromine (2.5 mL, 49 mmol). The reaction mixture was stirred for 15 hours at room temperature, and then concentrated under dry nitrogen. To the crude material in ethanol (30 mL) was added pyridin-2-amine (5.2 g, 55 mmol). The reaction mixture was heated at 60°C for 3 hours. The ethanol was evaporated, and the remainder was partitioned between EtOAc and water. The organic layer was dried, filtered through a short plug of silica gel, then concentrated under reduced pressure, and purified by silica gel chromatography to provide ethyl 2-(trifluoromethyl)imidazo[l,2-a]pyridine-3-carboxylate as a white solid (5.3 g, 42 %).
Step 2. To a suspension of NH4CI (2.67 g, 50 mmol) in toluene (20 mL) at 0°C was added AlMe-i (2M solution in toluene, 25 mL, 50 mmol) over about a 5 minute period followed by gas evolution. The suspension was stirred at 0°C for 5 minutes, then warmed to room temperature. A solution of ethyl 2-(trifluoromethyl)imidazo[l,2-a]pyridine-3carboxylate (2.58 g, 10 mmol) in toluene (50 mL) was added to the suspension. The reaction mixture was heated at 80°C for 72 hours and then cooled in an ice-bath, quenched with MeOH (100 mL) and NaOH (2 g, 50 mmol). The mixture was filtered through Celite, and concentrated to provide crude 2-(trifluoromethyl)imidazo[l,2-a]pyridine-3-carboximidamide as a brownish solid (2.3 g).
Step 3. A mixture of 2-(trifluoromethyl)imidazo[l,2-a]pyridine-3-carboximidamide (2.3 g, 10 mmol) and ethyl 3-(dimethylamino)acrylate (7.2 g, 50 mmol) in diphenyl ether (10
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!H NMR (500 MHz, DMSCMO δ ppm 9.61 (d, J = 6.9 Hz, 1H), 9.00 (d, J = 5.0 Hz, 1H), 7.94 (d, J = 8.8 Hz, 1H), 7.73 (d, J = 5.4 Hz, 1H), 7.69 (ddd, J = 8.7, 7.1, 1.3 Hz, 1H), 7.37 (td, J = 7.0, 1.1 Hz, 1H).
Step 4. To a solution of 3-(4-chloropyrimidin-2-yl)-2-(trifluoromethyl)imidazo[l,2a]pyridine (75 mg, 0.25 mmol) and benzo[d][l,3]dioxol-5-amine (69 mg, 0. 5 mmol) in THF (1 mL) at 0°C was added KOtBu (IM solution in THF, 1 mL, 1 mmol). After 10 minutes, the reaction mixture was quenched with HO Ac, then partitioned between EtO Ac and water. The organic portion was dried, then concentrated, and the remainder was purified by silica gel chromatography to provide the title compound as a tan solid (58 mg, 58 %).
’H NMR (500 MHz, DMSO-J6) δ ppm 9.70 (s, 1H), 9.43 (d, J = 6.6 Hz, 1H), 8.43 (d, J = 5.7 Hz, 1H), 7.84 (d, J = 9.1 Hz, 1H), 7.58 (ddd, J = 9.1, 6.9, 1.1 Hz, 1H), 7.37 (br. s., 1H), 7.17 (td, J = 6.9, 0.9 Hz, 1H), 6.95 (dd, J = 8.2, 1.9 Hz, 1H), 6.91 (d, J = 8.5 Hz, 1H), 6.72 (d, J = 6.0 Hz, 1H), 6.03 (s, 2H); MS m/z 400 [M+H]+.
Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 1 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
2 N-(2,3~dihydiO-l,4-benzodioxin-6-yl)-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidin-4amine ]H NMR (500 MHz, DMSO-O δ ppm 9.85 (dt, J = 6.9, 0.9 Hz, 1H), 9.45 (br. s, 1H), 8.36 (d, J = 5.7 Hz, 1H), 7.60 (dt, J = 8.8, 0.9 Hz, 1H), 7.38 (ddd, J = 8.8, 6.6, 1.3 Hz, 1H), 7.06 (d, J = 2.2 Hz, 1H), 6.95 - 6.98 (m, 2H), 6.87 (dd, J = 4.4, 3.5 Hz, 1H), 6.54 (d, J = 6.0 Hz, 1H), 4.25 - 4.30 (m, 4H), 2.75 (s, 3H); MS m/z 360 [M+H]+
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3 2-(2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidin-4-amine 'H NMR (500 MHz, DMSO-<7(i) δ ppm 10.06 (br. s, 1H), 9.81 (dt, J = 6.9, 1.1 Hz, 1H), 8.53 (d, J = 5.7 Hz, 1H), 7.90 (d, J = 8.5 Hz, 2H), 7.74 (d, J = 8.5 Hz, 2H), 7.63 (dt, J = 8.8, 1.1 Hz, 1H), 7.42 (ddd, J = 8.8, 6.6,1.3 Hz, 1H), 7.03 (td, J = 6.9, 1.3 Hz, 1H), 6.74 (d, J = 5.7 Hz, 1H), 2.78 (s, 3H); MS m/z 370 [M+H]+
4 N-(4-methoxyphenyl)-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidin-4-amine ]H NMR (500 MHz, DMSCW6) δ ppm 9.84 (d, J = 6.6 Hz, 1H), 9.44 (br. s, 1H), 8.35 (d, J = 6.0 Hz, 1H), 7.59 (dt, J = 8.8, 0.9 Hz, 1H), 7.47 (d, J = 8.5 Hz, 2H), 7.37 (ddd, J = 8.9, 6.9, 1.3 Hz, 1H), 6.97 - 7.00 (m, 2H), 6.95 (td, J = 6.9, 0.9 Hz, 1H), 6.52 (d, J = 5.7 Hz, 1H), 3.78 (s, 3H), 2.73 (s, 3H); MS m/z 332 [M+H]+
5 N-(4-chlorophenyl)-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidin-4-amine 'H NMR (500 MHz, DMSO-^) δ ppm 9.81 (d, J = 6.9 Hz, 1H), 9.78 (br. s, 1H), 8.45 (d, J = 5.7 Hz, 1H), 7.67 (d, J = 8.8 Hz, 2H), 7.61 (d, J - 8.8 Hz, 1H), 7.44 (s, 2H), 7.40 (ddd, J = 8.2, 6.9,1.3 Hz, 1H), 7.01 (td, J = 6.9, 1.3 Hz, 1H), 6.64 (d, J = 6.0 Hz, 1H), 2.74 (s, 3H); MS m/z 336 [M+H]+
6 2-(2-methylimidazo[l,2-a]pyridin-3-yl)-N-phenylpyrimidin-4-amine JH NMR (500 MHz, DMSO-^) δ ppm 9.85 (dt, J = 6.9, 0.9 Hz, 1H), 9.65 (br. s, 1H), 8.42 (d, J = 5.7 Hz, 1H), 7.59 - 7.64 (m, 3H), 7.36 - 7.43 (m, 3H), 7.11 (tt, J = 7.4, 0.9 Hz, 1H), 6.98 (ddd, J = 7.5, 5.5, 0.9 Hz, 1H), 6.63 (d, J = 6.0 Hz, 1H), 2.75 (s, 3H); MS m/z 302 [M+H]+
7 2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidin4-amine ‘bl NMR (500 MHz, DMSO-</6) δ ppm 10.25 (br. s, 1H), 9.36 (d, J = 6.9 Hz, 1H), 8.59 (d, J = 5.7 Hz, 1H), 7.92 (d, J = 8.5 Hz, 2H), 7.86 (d, J = 9.1 Hz, 1H), 7.67 (d, J = 8.5 Hz, 2H), 7.60 (ddd, J = 9.1, 6.9, 1.1 Hz, 1H), 7.21 (td, J = 6.9, 1.3 Hz, 1H), 6.92 (d, J = 5.7 Hz, 1H); MS m/z 424 [M+H]+
8 N-(4-chlorophenyl)-2-[2-(trifluoromethyl)imidazo[ 1,2-a]pyridin-3-yl]pyrimidin-4-amine JH NMR (500 MHz, DMSO-Jrt) δ ppm 9.95 (br. s., 1H), 9.37 (d, J = 6.9 Hz, 1H), 8.52 (d, J = 5.7 Hz, 1H), 7.85 (d, J = 8.8 Hz, 1H), 7.71 (d, J = 8.5 Hz, 2H), 7.59 (t, J = 7.6 Hz, 1H), 7.39 (d, J = 8.5 Hz, 2H), 7.20 (t, J = 6.8 Hz, 1H), 6.83 (d, J = 6.0 Hz, 1H); MS m/z 390 [M+H]+
9 N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine ‘H NMR (500 MHz, DMSCMJ δ ppm 9.75 (br. s, 1H), 9.41 (d, J = 6.6 Hz, 1H), 8.45 (d, J = 6.0 Hz, 1H), 7.84 (d, J = 9.1 Hz, 1H), 7.58 (t, J = 6.9 Hz, 1H), 7.53 (d, J == 7.6 Hz, 2H), 7.26 (d, J = 7.6 Hz, 1H), 7.17 (d, J = = 6.9 Hz, 2H), 6.77 (d, J = 5.7 Hz, 1H), 2.31 (s, 3H); MS m/z 370 [M+H]+
10 N-(4-bromophenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine !H NMR (500 MHz, DMSO-iZ6) δ ppm 9.97 (br. s, 1H), 9.37 (d, J = 6.9 Hz, 1H), 8.52 (d, J = 6.0 Hz, 1H), 7.85 (d, J = 8.8 Hz, 1H), 7.66 (d, J = 8.5 Hz, 2H), 7.59 (dd, J = 8.0, 6.9 Hz, 1H), 7.51 (d, J = 8.5 Hz, 2H), 7.20 (t, J == 6.9 Hz, 1H), 6.83 (d, J = 6.0 Hz, 1H); MS m/z 435 [M+H]+
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Cpd Name & Data
11 N-[4-(difluoromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine JH NMR (500 MHz, CHLOROFORM-<7) δ ppm 9.52 (dt, J - 7.3, 0.9 Hz, 1H), 8.38 (d, J = 6.0 Hz, 1H), 7.72 (dt, J == 9.1, 0.9 Hz, 1H), 7.30 - 7.37 (m, 3H), 7.11 (d, J - 8.8 Hz, 2H), 6.93 (td, J = 6.9, 1.3 Hz, 1H), 6.87 (br. s., 1H), 6.54 (d, J = 6.0 Hz, 1H), 6.46 (t, J = 73.8 Hz, 1H); MS m/z 422 [M+H]+
12 N-(4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine JH NMR (500 MHz, CHLOROFORM-<7) δ ppm 9.63 (dt, J = 7.3, 0.9 Hz, 1H), 8.40 (d, J = 6.0 Hz, 1H), 7.79 (dt, J = 9.1, 0.9 Hz, 1H), 7.41 (ddd, J = 9.0, 6.8, 1.3 Hz, 1H), 7.24 - 7.33 (m, 2H), 7.00 (td, J = 6.9, 0.9 Hz, 1H), 6.94 - 6.98 (m, 2H), 6.91 (br. s, 1H), 6.50 (d, J = 6.0 Hz, 1H), 3.87 (s, 3H); MS m/z 386 [M+H]+
13 2-[6-chloro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidin-4-amine 'bl NMR (500 MHz, DMSO-r/6) δ ppm 10.24 (br. s., 1H), 9.56 - 9.72 (m, 1H), 8.60 (d, J == 5.4 Hz, 1H), 7.83 - 7.98 (m, 3H), 7.63 - 7.74 (m, 3H), 6.90 (d, J = 5.4 Hz, 1H); MS m/z 458 [M+H]+
14 2-[6-chloro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethoxy)phenyl]pyrimidin-4-amine ’ll NMR (500 MHz, CHLOROFORM-d) δ ppm 9.72 - 9.82 (m, 1H), 8.49 (d, J = 6.0 Hz, 1H), 7.65 - 7.77 (m, 1H), 7.46 (dd, J = 9.0, 2.7 Hz, 2H), 7.39 (dd, J = 9.6, 2.0 Hz, 1H), 7.29 (d, J = 8.5 Hz, 2H), 6.84 (br. s, 1H), 6.64 (d, J = 6.0 Hz, 1H); MS m/z 474 [M+H]+
15 N-(4-bromophenyl)-2-[6-chloro-2-(trifluoromethyl)imidazo[ 1,2-a]pyridin-3 -yljpyrimidin4-amine *H NMR (500 MHz, DMSO-J6) δ ppm 9.96 (br. s, 1H), 9.60 (dd, J = 2.0, 0.8 Hz, 1H), 8.52 (d, J = 6.0 Hz, 1H), 7.92 (dd, J = 9.6, 0.8 Hz, 1H), 7.66 (dd, J = 9.6, 2.0 Hz, 1H), 7.61 - 7.64 (m, 2H), 7.50 - 7.55 (m, 2H), 6.81 (d, J = 6.0 Hz, 1H); MS m/z 469 [M+H]+
16 2-[6-chloro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(difluoromethoxy)phenyl]pyrimidin-4-amme !H NMR (500 MHz, CHLOROFORM-t/) δ ppm 9.60 - 9.78 (m, 1H), 8.40 (dd, J = 6.0, 0.9 Hz, 1H), 7.66 (dd, J = 9.5, 0.6 Hz, 1H), 7.34 (dd, J = 8.8, 2.5 Hz, 2H), 7.31 (dd, J = 9.6, 2.0 Hz, 1H), 7.13 (d, J = 8.8 Hz, 2H), 6.76 (br. s, 1H), 6.54 (d, J = 6.0 Hz, 1H), 6.46 (t, J = 74.4 Hz, 1H); MS m/z 456 [M+H]+
17 N-(4-chlorophenyl)-2-[6-chloro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin- 4-amine *H NMR (500 MHz, CHFOROFORM-r/) δ ppm 9.59 - 9.75 (m, 1H), 8.41 (dd, J - 6.0, 0.9 Hz, 1H), 7.66 (dd, J = 9.6, 0.8 Hz, 1H), 7.23 - 7.36 (m, 5H), 6.74 (br. s, 1H), 6.55 (dd, J = 6.0, 1.3 Hz, 1H); MS m/z 425 [M+H]+
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Cpd Name & Data
18 2-[2-methyl-6-(trifluoromethyl)imidazo[l ,2-a]pyridin-3-yl]-N-[4- (trifluoromethyl)phenyl]pyrimidin-4-amine !H NMR (500 MHz, DMSO-i/Q δ ppm 10.33 (br. s, 1H), 10.26 (s, 1H), 8.59 (d, J = 6.0 Hz, 1H), 7.98 (d, J = 9.1 Hz, 1H), 7.88 (d, J = 11.0 Hz, 1H), 7.86 (d, J = 8.5 Hz, 2H), 7.70 (d, J = 8.5 Hz, 2H), 6.85 (d, J = 6.0 Hz, 1H), 2.86 (s, 3H); MS m/z 438 [M+H]+
19 N-(4-bromophenyl)-2-[2-methyl-6-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrirnidin- 4-amine *H NMR (500 MHz, DMSO-4) δ ppm 10.30 (s, 1H), 10.07 (br. s, 1H), 8.52 (d, J = 6.0 Hz, 1H), 7.99 (d, J = 8.8 Hz, 1H), 7.87 - 7.96 (m, 1H), 7.60 (d, J = 8.8 Hz, 2H), 7.53 (d, J - 8.8 Hz, 2H), 6.78 (d, J = 6.0 Hz, 1H), 2.83 (s, 3H); MS m/z 449 [M+H]+
20 N-(4-methylphenyl)-2- [2-methyl-6-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 -yl]pyrimidin4-amine ’H NMR (500 MHz, DMSO-^) δ ppm 10.28 (s, 1H), 9.83 (br. s, 1H), 8.44 (d, J = 6.0 Hz, 1H), 7.92 (d, J = 9.3 Hz, 1H), 7.80 (d, J = 9.3 Hz, 1H), 7.47 (d, J = 8.2 Hz, 2H), 7.17 (d, J = 8.2 Hz, 2H), 6.70 (d, J = 6.0 Hz, 1H), 2.81 (s, 3H), 2.30 (s, 3H); MS m/z 384 [M+H]+
21 2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-(4-methylphenyl)pyrimidin4-amine ’H NMR (500 MHz, DMSCMO δ ppm 9.78 (s, 1H), 9.63 (br. s, 1H), 8.44 (d, J = 6.0 Hz, 1H), 7.94 (dd, J = 10.1, 5.4 Hz, 1H), 7.70 (ddd, J = 10.7, 7.9, 2.5 Hz, 1H), 7.49 (d, J = 8.0 Hz, 2H), 7.18 (d, J = 8.0 Hz, 2H), 6.74 (d, J = 8.8 Hz, 1H), 2.30 (s, 3H); MS m/z 388 [M+H]+
22 . 2-[6-fluoro-2-(trifluoromethyl)imidazo[l ,2-a]pyridin-3-yl]-N-(4methoxyphenyl)pyrimidin-4-amine ’H NMR (500 MHz, DMSO-r/Q δ ppm 9.63 (br. s, 1H), 8.41 (d, J = 5.7 Hz, 1H), 7.94 (dd, J = 9.9, 5.2 Hz, 1H), 7.69 (ddd, J = 10.0, 7.8, 2.4 Hz, 1H), 7.48 (d, J = 8.2 Hz, 2H), 6.96 (d, J - 8.8 Hz, 2H), 6.75 - 6.82 (m, 1H), 6.68 (d, J - 6.0 Hz, 1H), 3.77 (s, 3H); MS m/z 404 [Mil·!]'
23 2-[5chloro-l-methyl-2-(trifluoromethyl)-lH-indol-3-yl]-N-(4-methoxyphenyl)pyrimidin-4amine ’H NMR (500 MHz, CHLOROFORM-rZ) δ ppm 8.27 (d, J = 6.3 Hz, 1H), 7.87 (d, J = 1.9 Hz, 1H), 7.56 (br. s, 1H), 7.26 (dd, J = 8.5, 1.9 Hz, 1H), 7.20 (d, J = 8.8 Hz, 1H), 7.07 (d, J = 8.8 Hz, 2H), 6.73 - 6.80 (m, 2H), 6.42 (d, J = 6.0 Hz, 1H), 3.78 (s, 3H), 3.74 (s, 3H); MS m/z 433 [M+H]+
24 2-[5-chloro-l-methyl-2-(trifluoromethyl)-lH-indol-3-yl]-N-[4(difluoromethoxy)phenyl]pyrimidin-4-amine *H NMR (500 MHz, DMSO-O δ ppm 10.47 (br. s, 1H), 8.47 (d, J = 6.6 Hz, 1H), 7.98 (d, J = 2.2 Hz, 1H), 7.84 (d, J = 9.1 Hz, 1H), 7.74 (d, J = 8.8 Hz, 2H), 7.50 (dd, J = 8.8, 1.9 Hz, 1H), 7.16 (d, J = 8.8 Hz, 2H), 7.18 (t, J = 74.4 Hz, 1H), 6.90 (d, J = 6.3 Hz, 1H), 4.00 (s, 3H); MS m/z 469 [M+H]+
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25 N-(4-bromophenyl)-2-[5-chloro-l-methyl-2-(trifluoromethyl)-lH-indol-3-yl]pyrimidin-4amine ]H NMR (500 MHz, DMSO-i/^) δ ppm 10.24 (br. s, 1H), 8.49 (d, J = 6.0 Hz, 1H), 7.98 (d, J = 2.2 Hz, 1H), 7.83 (d, J = 8.8 Hz, 1H), 7.70 (d, J = 8.8 Hz, 2H), 7.43 - 7.52 (m, J = 8.5 Hz, 3H), 6.87 (d, J = 6.0 Hz, 1H), 4.00 (s, 3H); MS m/z 482 [M+H]+
26 N-(4-bromophenyl)-2-(6-fluoro-2-phenylimidazo[l,2-a]pyridin-3-yl)pyrimidin-4-amine 'll NMR (500 MHz, DMSO-gQ δ ppm 9.75 (br. s., 1H), 9.55 (d, J == 3.2 Hz, 1H), 8.49 (d, J = 5.4 Hz, 1H), 7.83 (dd, J = 8.8, 5.0 Hz, 1H), 7.67 (d, J = 7.9 Hz, 2H), 7.57 (td, J = 9.1, 1.6 Hz, 1H), 7.31 - 7.46 (m, J = 7.6 Hz, 3H), 7.01 - 7.21 (m, 4H), 6.72 (d, J = 5.7 Hz, 1H); MS m/z 461 [M+H]+
27 2-(6-fluoro-2-phenylimidazo[l,2-a]pyridin-3-yl)-N-(4-methylphenyl)pyrimidin-4-amine !H NMR (500 MHz, DMSO-t/d) δ ppm 9.88 (br. s, 1H), 9.49 - 9.61 (m, 1H), 8.37 (d, J = 6.0 Hz, 1H), 7.90 (dd, J = 9.9, 5.2 Hz, 1H), 7.66 - 7.75 (m, 3H), 7.39 - 7.49 (m, 3H), 7.14 (d, J = 8.2 Hz, 2H), 6.94 (d, J = 8.2 Hz, 2H), 6.74 (d, J = 6.3 Hz, 1H), 2.23 (s, 3H); MS m/z 396 [M+H]+
29 N-(2,3-dihydro-l,4-benzodioxin-6-yl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine !H NMR (500 MHz, DMSO-i/6) δ ppm9.63 (s, 1H), 8.42 (d, J = 5.7 Hz, 1H), 7.84 (dt, J = 9.1, 0.9 Hz, 1H), 7.58 (ddd, J = 9.0, 6.8, 1.3 Hz, 1H), 7.22 (br. s., 1H), 7.15 (td, J = 6.9, 1.3 Hz, OH), 7.01 (dd, J = 8.5, 2.2 Hz, 1H), 6.84 (d, J = 8.8 Hz, 1H), 6.71 (d, J = 6.0 Hz, 1H), 4.20 - 4.29 (m, 4H); MS m/z 410 [M+H]+
30 N-(6-methoxypyridin-3-yl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine ’H NMR (500 MHz, CHLOROFORM-^/) δ ppm 9.53 (d, J = 6.9 Hz, 1H), 8.34 (d, J = 5.7 Hz, 1H), 8.10 (d, J = 2.5 Hz, 1H), 7.69 (dt, J = 9.1, 0.9 Hz, 1H), 7.65 (d, J = 7.6 Hz, 1H), 7.32 (ddd, J = 9.0, 6.8, 1.3 Hz, 1H), 6.91 (td, J = 7.0, 1.3 Hz, 2H), 6.75 (d, J = 8.5 Hz, 1H), 6.40 (d, J = 6.0 Hz, 1H), 3.90 (s, 3H); MS m/z 387 [M+H]+
31 N2,N2-dimethyl-N5- {2-[2-(trifluoromethyl)imidazo[ 1,2-a]pyridin-3-yl]pyrimidin-4yl }pyridine-2,5-diamine !H NMR (500 MHz, CHLOROFORM-d) δ ppm 9.55 (d, J = 6.9 Hz, 1H), 8.29 (d, J = 6.0 Hz, 1H), 8.10 (d, J = 2.5 Hz, 1H), 7.70 (d, J = 9.1 Hz, 1H), 7.51 (br. s, 1H), 7.32 (ddd, J = 9.1, 6.9, 1.1 Hz, 1H), 6.92 (td, J = 6.9, 0.9 Hz, 1H), 6.81 (br. s, OH), 6.51 (d, J = 9.1 Hz, 1H), 6.35 (d, J = 5.4 Hz, 1H), 3.08 (s, 6H); MS m/z 400 [M+H]+
32 2-[6-bromo-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidin-4-amine !H NMR (500 MHz, DMSO-i/6) δ ppm 10.25 (br. s, 1H), 9.66 (dd, J = 1.9, 0.9 Hz, 1H), 8.60 (d, J = 6.0 Hz, 1H), 7.91 (d, J = 8.5 Hz, 2H), 7.87 (dd, J = 9.6, 0.8 Hz, 1H), 7.74 (dd, J = 9.5, 1.9 Hz, 1H), 7.69 (d, J = 8.8 Hz, 2H), 6.90 (d, J = 6.0 Hz, 1H); MS m/z 503 [M+H]+
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33 2-[6-bromo-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-(4methoxyphenyl)pyrimidin-4-amine ’H NMR (500 MHz, CHLOROFORM-ri) δ ppm 9.70 - 9.86 (m, 1H), 8.32 (d, J = 4.7 Hz, 1H), 7.60 (d, J = 9.5 Hz, 1H), 7.40 (dd, J = 9.6, 1.7 Hz, 1H), 7.22 (d, J = 8.5 Hz, 2H), 6.89 (d, J = 8.8 Hz, 2H), 6.47 (br. s, 1H), 3.78 (s, 3H); MS m/z 465 [M+H]+
34 N-(3-fluoiO-4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine ’H NMR (500 MHz, DMSO-t/Q δ ppm 9.77 (s, 1H), 9.35 (d, J = 6.9 Hz, 1H), 8.42 (d, J = 6.0 Hz, 1H), 7.80 (d, J = 9.1 Hz, 1H), 7.68 (d, J = 13.6 Hz, 1H), 7.53 (ddd, J = 9.1, 6.9, 1.3 Hz, 1H), 7.17 - 7.23 (m, 1H), 7.13 (td, J = 6.9, 1.1 Hz, 1H), 7.13 (td, J = 6.9, 0.9 Hz, 1H), 7.10 (t, J = 9.1 Hz, 1H), 6.70 (d, J = 6.0 Hz, 1H), 3.78 (s, 3H); MS m/z 404 [M+H]+
35 N-(3-chloro-4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine ’H NMR (500 MHz, DMSO-JQ δ ppm 9.80 (s, 1H), 9.40 (d, J = 6.9 Hz, 1H), 8.47 (d, J = 6.0 Hz, 1H), 7.88 -7.92 (m, 1H), 7.85 (dt, J = 9.1, 1.0 Hz, 1H), 7.59 (ddd, J = 9.1, 6.6, 1.3 Hz, 1H), 7.43 (dd, J = 8.8, 2.8 Hz, 1H), 7.18 (td, J = 6.9, 1.3 Hz, 1H), 7.15 (d, J = 9.1 Hz, 1H), 6.74 (d, J = 6.0 Hz, 1H), 3.85 (s, 3H); MS m/z 420 [M+H]+
36 N-(3-chloro-4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin4-amine 'bl NMR (500 MHz, DMSO-Jrt) δ ppm 9.92 (s, 1H), 9.38 (d, J = 7.3 Hz, 1H), 8.51 (d, J = 6.0 Hz, 1H), 7.94 (d, J = 1.9 Hz, 1H), 7.86 (dt, J = 9.1, 1.1 Hz, 1H), 7.59 (ddd, J = 9.1, 6.9, 1.3 Hz, 1H), 7.41 (dd, J = 8.2, 2.2 Hz, 1H), 7.31 (d, J = 8.5 Hz, 1H), 7.20 (td, J = 6.9, 1.3 Hz, 1H), 6.80 (d, J = 5.7 Hz, 1H), 2.30 (s, 3H); MS m/z 404 [M+H]+
37 N-(4-ethoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine ’H NMR (500 MHz, DMSO-d6) δ ppm 9.64 (br. s, 1H), 9.43 (br. s, 1Ή), 8.41 (d, J = 6.0 Hz, 1H), 7.84 (dt, J = 9.1, 1.3 Hz, 1H), 7.57 (ddd, J = 9.1, 6.9, 1.1 Hz, 1H), 7.50 (d, J = 8.5 Hz, 1H), 7.16 (t, J = 6.5 Hz, 1H), 6.93 (d, J = 8.8 Hz, 2H), 6.69 (d, J = 6.0 Hz, 1H), 4.02 (q, J = 6.9 Hz, 2H), 1.34 (t, J = 6.9 Hz, 3H); MS m/z 400 [M+H]+
38 N-[4-(propan-2-yl)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine ‘H NMR (500 MHz, DMSO-ri6) δ ppm 9.76 (s, 1H), 9.41 (d, J = 6.9 Hz, 1H), 8.45 (d, J = 6.0 Hz, 1H), 7.85 (dt, J = 9.1, 0.9 Hz, 1H), 7.58 (ddd, J = 8.8, 6.6, 1.3 Hz, 1H), 7.55 (d, J = 8.5 Hz, 2H), 7.23 (d, J = 8.5 Hz, 2H), 7.16 (td, J = 6.9, 0.9 Hz, 1H), 6.77 (d, J = 6.0 Hz, 1H), 2.89 (spt, J = 6.9 Hz, 1H), 1.21 (d, J = 6.9 Hz, 7H); MS m/z 398 [M+H]+
39 N-[4-(lH-pyrazol-l-yl)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidm-4-amine ]H NMR (500 MHz, DMSO-r/Q δ ppm 9.98 (s, 1H), 9.42 (d, J = 7.3 Hz, 1H), 8.51 (d, J = 5.7 Hz, 1H), 8.48 (d, J = 2.2 Hz, 1H), 7.86 (td, J = 9.1, 1.3 Hz, 1H), 7.76 - 7.84 (m, J = 3.5 Hz, 4H), 7.73 (d, J = 1.6 Hz, 1H), 7.59 (ddd, J = 9.0, 6.8, 1.3 Hz, 1H), 7.20 (td, J = 6.9, 1.3 Hz, 1H), 6.84 (d, J = 6.0 Hz, 1H), 6.54 (t, J = 1.9 Hz, 1H); MS m/z 422 [M+H]+
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Cpd Name & Data
45 N-(4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4-amine !H NMR (500 MHz, Acetone-^) δ ppm 9.53 (br. s., 1H), 9.16 (d, J = 1.3 Hz, 1H), 8.81 (s, 1H), 8.38 (d, J = 6.0 Hz, 1H), 8.03 (d, J = 4.7 Hz, 1H), 7.46 (d, J = 8.5 Hz, 2H), 6.95 (d, J = 9.1 Hz, 2H), 6.70 (dd, J = 8.2, 2.5 Hz, 1H), 3.79 (s, 3H); MS m/z 387 [M+H]+
46 2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidin4-amine !H NMR (500 MHz, Acetone-^) δ ppm 9.41 - 9.49 (m, 1H), 9.20 (br. s, 1H), 8.49 (dd, J = 6.0, 2.2 Hz, 1H), 8.02 - 8.12 (m, 1H), 7.83 - 7.92 (m, 2H), 7.58 (d, J = 8.5 Hz, 2H), 6.93 7.32 (m, 2H); MS m/z 425 [M+H]+
47 N-(4-chlorophenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4-amine ΪΙ NMR (500 MHz, Acetone-r/6) δ ppm 9.53 (dd, J = 4.9, 1.4 Hz, 1H), 9.25 (d, J = 1.3 Hz, 1H), 9.20 (br. s., 1H), 8.55 (d, J = 6.0 Hz, 1H), 8.15 (d, J = 4.7 Hz, 1H), 7.70 - 7.81 (m, 2H), 7.42 (d, J = 8.8 Hz, 2H), 6.91 (d, J = 6.0 Hz, 1H); MS m/z 391 [M+H]+
48 2-[6-methoxy-2-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 -yl] -N- [4(trifluoromethyl)phenyl]pyrimidin-4-amine 'll NMR (500 MHz, DMSO-ri0) δ ppm 10.31 (br. s, 1H), 9.02 (d, J = 2.5 Hz, 1H), 8.65 (d, J = 5.7 Hz, 1H), 7.96 (d, J = 8.5 Hz, 2H), 7.85 (d, J = 10.4 Hz, 1H), 7.74 (d, J = 8.5 Hz, 2H), 7.45 (dd, J = 9.8, 2.5 Hz, 1H), 6.95 (d, J = 6.0 Hz, 1H), 3.66 (s, 3H); MS m/z 454 [M+H]+
49 2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethoxy)phenyl]pyrimidin-4-amine ]H NMR (500 MHz, DMSO-Jrt) δ ppm 9.65 (br. s, 1H), 8.96 - 9.06 (m, 1H), 8.42 (d, J = 5.7 Hz, 1H), 7.76 (d, J = 9.8 Hz, 1H), 7.51 (d, J = 8.5 Hz, 2H), 7.36 (dd, J = 9.6, 2.4 Hz, 1H), 6.93 (d, J = 8.8 Hz, 2H), 6.69 (d, J = 6.0 Hz, 1H), 3.75 (s, 3H); MS m/z 470 [M+H]+
50 N-(4-methoxyphenyl)-2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine *H NMR (500 MHz, DMSO-J6) δ ppm 10.04 (br. s, 1H), 8.97 (d, J - 1.9 Hz, 1H), 8.54 (d, J = 5.7 Hz, 1H), 7.75 - 7.79 (m, 3H), 7.38 (dd, J = 9.1, 2.2 Hz, 1H), 7.34 (d, J = 8.5 Hz, 2H), 6.82 (d, J = 6.0 Hz, 1H), 3.59 (s, 3H), 3.33 (s, 3H); MS m/z 416 [M+H]+
51 N-[4-(difluoromethoxy)phenyl]-2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine !H NMR (500 MHz, DMSO-c/Q δ ppm 9.90 (br. s, 1H), 8.98 (d, J = 1.9 Hz, 1H), 8.50 (d, J = 6.0 Hz, 1H), 7.78 (d, J = 9.5 Hz, 1H), 7.69 (d, J = 8.8 Hz, 2H), 7.37 (dd, J = 9.8, 2.5 Hz, 1H), 7.17 (d, J = 8.8 Hz, 2H), 7.19 (t, J = 74.4 Hz, 1H), 6.78 (d, J = 5.7 Hz, 1H), 3.61 (s, 3H); MS m/z 452 [M+H]+
53 N-[4-(difluoromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3- yl] pyrimidin-4- amine !H NMR (500 MHz, Acetone-^) δ ppm 9.74 (dd, J = 4.9, 1.4 Hz, 1H), 9.44 (d, J = 1.6 Hz, 1H), 9.30 (br. s., 1H), 8.72 (d, J = 6.0 Hz, 1H), 8.32 (d, J = 4.7 Hz, 1H), 7.89 - 8.00 (m, 2H), 7.42 - 7.52 (m, 2H), 7.07 (dd, J = 6.0, 1.6 Hz, 1H), 7.20 (t, J = 74.4 Hz, 1H); MS m/z 423 [M+H]+
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Cpd Name & Data
54 2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidin-4-amine ’H NMR (500 MHz, DMSO-d(i) δ ppm 10.25 (br. s, 1H), 9.58 (ddd, J = 5.7, 1.9, 0.9 Hz, 1H), 8.59 (d, J = 6.0 Hz, 1H), 7.97 (ddd, J = 9.8, 5.4, 0.9 Hz, 1H), 7.90 (d, J = 8.5 Hz, 2H), 7.73 (ddd, J = 9.9, 7.7, 2.5 Hz, 1H), 7.69 (d, J = 8.8 Hz, 2H), 6.90 (d, J = 6.0 Hz, 1H); MS m/z 442 [M+H]+
55 N-[4-(difluoromethoxy)phenyl]-2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine *H NMR (500 MHz, Acetone-<76) δ ppm 9.75 (dd, J = 5.5, 2.0 Hz, 1H), 9.10 (br. s, 1H), 8.51 (d, J = 5.7 Hz, 1H), 7.84 (ddd, J = 9.8, 5.4, 0.9 Hz, 1H), 7.71 - 7.76 (m, 2H), 7.60 (ddd, J = 10.0, 7.6, 2.5 Hz, 1H), 7.22 - 7.26 (m, 2H), 6.99 (t, J = 74.1 Hz, 1H), 6.83 (d, J = 6.0 Hz, 1H); MS m/z 440 [M+H]+
56 N-[4-(trifluoromethyl)phenyl]-2-[2-(trifluoromethyl)pyrazolo[l,5-a]pyridin-3yl]pyrimidin-4-amine rH NMR (500 MHz, CHLOROFORM-d) δ ppm 10.03 (br. s, 1H), 8.48 (d, J = 6.9 Hz, 1H), 8.21 - 8.36 (m, 1H), 8.00 - 8.15 (m, 1H), 7.65 - 7.73 (m, 2H), 7.52 (d, J = 8.2 Hz, 2H), 7.39 (t, J = 7.7 Hz, 1H), 7.06 - 7.12 (m, 1H), 7.03 (t, J = 6.8 Hz, 1H); MS m/z 424 [M+H]+
60 N-(4-methoxyphenyl)-2-[2-(trifluoromethyl)pyrazolo[l,5-a]pyridin-3-yl]pyrimidin-4amine !H NMR (500 MHz, CHLOROFORM-d) δ ppm 8.49 (d, J = 6.6 Hz, 1H), 8.03 - 8.31 (m, 2H), 7.30 - 7.55 (m, 3H), 7.00 - 7.12 (m, 2H), 6.79 - 6.87 (m, 3H), 3.76 (s, 3H); MS m/z 386 [M+H]+
62 N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4-amine ’H NMR (500 MHz, Acetone-^) δ ppm 9.58 (d, J = 3.8 Hz, 1H), 9.23 (d, J = 1.6 Hz, 1H), 8.95 (br. s., 1H), 8.48 (d, J = 6.0 Hz, 1H), 8.10 (d, J = 4.7 Hz, 1H), 7.53 (d, J = 8.5 Hz, 2H), 7.25 (d, J = 8.2 Hz, 2H), 6.83 (d, J = 6.0 Hz, 1H), 2.37 (s, 3H); MS m/z 371 [M+H]+
118 2-(imidazo[l ,2-a]pyridin-3-yl)-N-[4~(trifluoromethyl)phenyl]pyrimidiil-4-amine ’H NMR (500 MHz, DMSO-d6) δ ppm 10.10 (s, 1H), 9.92 (d, J = 7.3 Hz, 1H), 8.51 (app. s, 1H), 8.48 (d, J = 5.7 Hz, 1H), 8.00 (d, J = 8.5 Hz, 2H), 7.75 - 7.86 (m, 3H), 7.46 (ddd, J = 9.1, 6.6, 0.9 Hz, 1H), 7.14 (td, J = 6.9, 1.1 Hz, 1H), 6.74 (d, J = 6.0 Hz, 1H); MS m/z 356 [M+H]+
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Example 2
N-(3-chloro-4-methoxyphenyl)-2-(2-methyl-177-benzimidazol-l-yl)pyrimidin-4-amine (Cpd 40)
Figure AU2013348009C1_D0151
Stepl. 3-Chloro-4-methoxyaniline (2.07 g, 13.1 mmol), 2,4-di chloropyrimidine (1.95 g, 13.1 mmol) and triethylamine (2.1 mL, 15 mmol) were mixed in isopropanol (10 mL). The mixture was heated at 100°C for 13 hours, then partially concentrated, diluted with water, and made basic with K2CO3. The precipitate was filtered, then washed with water, followed by hexane. The major isomer, 2-chloro-N-(3-chloro-4-methoxyphenyl)pyrimidin-4amine (2.07 g, 59 %) was recrystallized from methanol as a white solid.
’H NMR (500 MHz, DMSO-JQ δ ppm 9.99 (br. s, 1H), 8.15 (d, J = 6.0 Hz, 1H), 7.73 (br. s., 1H), 7.47 (d, J = 8.2 Hz, 1H), 7.19 (d, J = 8.8 Hz, 1H), 6.69 (d, J = 5.7 Hz, 1H), 3.85 (s, 3H).
Step 2. 2-Chloro-N-(3-chloro-4-methoxyphenyl)pyrimidin-4-amine (84 mg, 0.31 mmol), 2-methyl-lH-benzo[d]imidazole (82 mg, 0.62 mmol) and K2CO3 (86 mg, 0.62 mmol) were mixed in DMF (2 mL). The reaction mixture was heated at 120°C for 3 days, then cooled, partitioned between water and EtOAc, and purified by silica gel chromatography to provide the title compound as a white solid (29 mg, 26%).
JH NMR (500 MHz, DMSO-O δ ppm 9.94 (s, 1H), 8.42 (d, J = 5.7 Hz, 1H), 8.03 - 8.10 (m, 1H), 7.82 - 7.90 (m, 1H), 7.61 (d, J = 7.3 Hz, 1H), 7.40 - 7.45 (m, 1H), 7.20 - 7.29 (m, 2H), 7.18 (d, J = 8.8 Hz, 1H), 6.73 (d, J = 5.7 Hz, 1H), 3.86 (s, 3H), 2.79 (s, 3H); MS m/z 366 [M+H]+.
Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 2 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
1 N-(4-methoxyphenyl)-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-amine 'H NMR (500 MHz, DMSO-J6) δ ppm 9.79 (br. s., 1H), 8.36 (d, J = 5.4 Hz, 1H), 7.95 8.17 (m, 1H), 7.59 (d, J = 7.9 Hz, 1H), 7.42 - 7.54 (m, 2H), 7.17 - 7.33 (m, 2H), 6.96 (d, J = 8.2 Hz, 2H), 6.68 (d, J = 5.0 Hz, 1H), 3.76 (s, 3H), 2.77 (s, 3H); MS m/z 332 [M+H]+
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Cpd Name & Data
41 2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyririiidin-4-amine ]H NMR (500 MHz, DMSO-ri6) δ ppm 10.37 (s, 1H), 8.55 (d, J = 5.7 Hz, 1H), 8.01 - 8.06 (m, 1H), 7.90 (d, J = 8.5 Hz, 1H), 7.72 (d, J = 8.5 Hz, 2H), 7.61 - 7.65 (m, 1H), 7.26 (app. quind, J = 7.3, 1.4 Hz, 2H), 6.91 (d, J = 5.7 Hz, 1H), 2.81 (s, 3H); MS m/z 370 [M+H]+
61 N-[4-(difluoromethoxy)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidin-4-amine ‘H NMR (500 MHz, Methanol-ri4) δ ppm 8.32 (1H, d, J = 5.5 Hz), 8.06 (1H, d, J = 8 Hz), 7.59 (3H, d, J = 8 Hz), 7.26 (2H, m), 7.14 (2H, d, J = 8 Hz), 7.0 (1H, t, J = 74 Hz), 6.69 (1H, d, 1== 6 Hz), 2.82 (3H, s); MS m/z 368 [M+H]+
Example 3
N-(3-chloro-4-methoxyphenyl)-2-[2-(trifluoromethyl)-lH-benzimidazol-l-yl]pyrimidin-4amine (Cpd 42)
Figure AU2013348009C1_D0152
A mixture of 2-chloro-N-(3-chloro-4-methoxyphenyl)pyrimidin-4-amine (280 mg,
1.03 mmol) and benzene- 1,2-diamine (540 mg, 5 mmol) in isopropanol (5 mL) was heated in a microwave oven at 160°C for 10 minutes. The reaction mixture was diluted with water, extracted with EtOAc, then filtered through a short plug of silica gel, and concentrated to provide a first crude intermediate N2-(2-aminophenyl)-N4-(3-chloro-410 methoxyphenyl)pyrimidine-2,4-diamine. The first crude intermediate was dissolved in dichloromethane (5 mL), then trifluoroacetic anhydride was added in two portions (0.5 mL each). The reaction mixture was washed with an aqueous Nal lCCL solution, and purified by silica gel chromatography to provide a second crude intermediate N-(2-(4-(3-chloro-4methoxyphenylamino)-pyrimidin-2-ylamino)phenyl)-2,2,2-trifluoroacetamide.
To a solution of the second crude intermediate (71 mg, 0.16 mmol) in acetonitrile (2 mL) was added trifluoroacetic acid (0.5 mL). The mixture was heated in a microwave oven at 180°C for 1 hour and 45 minutes after which UPLC showed complete conversion. The final product was purified by silica gel chromatography to provide the title compound as a white solid (40 mg, 59%).
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PCT/US2013/071132 JH NMR (500 MHz, DMSO->) δ ppm 10.06 - 10.18 (m, 1H), 8.45 (d, J - 5.7 Hz, 1H), 8.02 (d, J = 8.2 Hz, 1H), 7.94 (d, J = 7.3 Hz, 1H), 7.83 - 7.90 (m, 1H), 7.52 - 7.56 (m, J = 8.2, 8.2, 1.3 Hz, 1H), 7.50 (td, > 7.9, 1.3 Hz, 1H), 7.43 (dd, J = 9.0, 2.7 Hz, 1H), 7.15 (d, J = 8.8 Hz, 1H), 6.86 (d, J = 6.0 Hz, 1H), 3.84 (s, 3H); MS m/z 420 [M+H]+.
Example 4
5-fluoro-N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine (Cpd 43)
Figure AU2013348009C1_D0153
Stepl: A mixture of 2,4-dichloro-5-fluoropyrimidine (1.00 g, 5.99 mmol), 4-toluidine (642 mg, 5.99 mmol) and K2CO3 (1.66 g, 12.0 mmol) in EtOH (10 mL) was stirred for 18 hours at 50°C. The mixture was filtered through Celite and purified by column chromatography to yield 2-chloro-5-fluoro-N-p-tolylpyrimidin-4-amine (1.19 g, 84%).
Step2: A mixture of 2-chloro-5-fluoro-N-p-tolylpyrimidin-4-amine (165 mg, 0.69 mmol), 3-(tributylstannyl)-2-(trifluoromethyl)imidazo[l,2-a]pyridine (300 mg, 0.63 mmol), Q-Phos (13.5 mg, 0.019 mmol) and PdCl2(allyl) (6.9 mg, 0.019 mmol) in dioxane (1.5 mL) was stirred for 2 hours at 90°C. The mixture was purified by column chromatography to yield the title compound (213 mg, 80%).
*H NMR (500 MHz, CHLOROFORM-;/) δ ppm 9.24 - 9.29 (1H, m) 8.29 (1H, d, >2.84 Hz) 7.66 - 7.71 (1H, m) 7.46 (2H, d, >8.51 Hz) 7.31 (1H, ddd, >9.14, 6.62, 1.26 Hz) 7.14 (2H, d, >8.20 Hz) 6.82 - 6.89 (2H, m) 2.30 (3H, s); MS m/z 388.2 [M+H]+.
Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 4 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
44 5-chloro-N-(4-methylphenyl)-2-[2-(trifhioromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin4-amine !H NMR (500 MHz, CHLOROFORM-J) δ ppm 9.34 - 9.42 (1H, m) 8.51 (1H, s) 7.80 (1H, dd, >9.14, 0.95 Hz) 7.49 (2H, d, >8.51 Hz) 7.41 (1H, ddd, >8.99, 6.78, 1.26 Hz) 7.20 - 7.27 (3H, m) 6.91 (1H, td, >6.94, 1.26 Hz) 2.42 (3H, s); MS m/z 404.2 [M+H]+
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Example 5
2-(6-fhioro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4-(trifluorornethyl)phenyl]pyrimidine4,6-diamine (Cpd 68)
Figure AU2013348009C1_D0154
Step 1. A mixture of 2,6-dichloropyrimidine-4-amine (3.78 g, 23.05 mmol) and DMAP (cat.) in dichloromethane (20 mL) was treated with di-Zer/-butyldicarbonatc (11.05 g, 50.71 mmol) at 0°C. After addition, the resulting mixture was stirred at ambient temperature overnight. The mixture was poured into ice-water (120 mL) and extracted with dichloromethane (150 mL). The organic phase was separated, washed with brine (100 mL), dried over MgSCL, then filtered and evaporated. The residual material was separated by filtering through a pad of silica gel (100 g) to afford di-teri-butyl (2,6-dichloropyrimidin-4yl)imidodicarbonate as an oil (7.55 g, 90%).
Step 2. A solution of di-Zer/-butyl (2,6-dichloropyrimidin-4-yl)imidodiearbonate (1.75 g, 4.81 mmol) and 4-trifluoromethylaniline (775.0 mg, 4.81 mmol) in THF (10 mL) was treated with potassium ZerZ-butoxide solution (IM in THF, 9.62 mL, 9.62 mmol) at 78°C. The mixture was allowed to stir and warm to 0°C over 20 minutes. The mixture was then poured into ice-water (120 mL) and extracted with dichloromethane (150 mL). The organic phase was separated, washed with brine (100 mL), dried over MgSCL, then filtered and evaporated. The residual material was separated by silica gel column chromatography (by eluting with hexane then 2% ethyl acetate-hexane) to afford di-ZerZ-butyl 6-chloro-2-(4(trifluoromethyl)phenylamino)pyrimidin-4-yliminodicarbonate (750.0 mg, 32% yield), and (by eluting with 4% ethyl acetate-hexane) di-ZerZ-butyl 2-chloro-6-(4(trifluoromethyl)phenylamino)pyrimidin-4-yliminodicarbonate (1.08 g, 46%).
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F
Figure AU2013348009C1_D0155
O
Figure AU2013348009C1_D0156
ACN
Figure AU2013348009C1_D0157
CsOAc, DMA
Figure AU2013348009C1_D0158
Step 3. 4-Fluoropyridin-2-amine (8.57 g, 76.44 mmol) and chloroacetone (12.99 g, 71.67 mmol) were pre-mixed and stirred in a 250 mL round bottom flask at 0°C for 15 minutes. The resulting mixture was diluted with acetonitrile (50 mL) and refluxed for overnight. The acetonitrile was evaporated, and ethyl ether (200 mL) was added to produce a precipate, which was collected by filtration. The solid was partitioned between dichloromethane (300 mL) and a saturated NaHCCh solution (250 mL). The organic layer was separated, dried over MgSCL, then filtered and concentrated under the reduced pressure. The residual material was separated by silica gel column chromatography (1:1 ethyl acetate10 hexane) to afford 6-fluoro-2-methylimidazo[l,2-a]pyridine (5.20 g, 46%) as a glassy solid.
*H NMR (500 MHz, CHLOROFORM-d) δ ppm 7.95 - 7.99 (m, 1H), 7.46 (dd, J= 5.04, 9.77 Hz, 1H), 7.34 (s, 1H), 6.99 - 7.06 (m, 1H), 2.44 (d, J= 0.63 Hz, 3H); MS m/z 151.0 (100) [M‘H]'.
Step 4. A mixture of 6-fluoro-2-methylimidazo[l,2-«]pyridine (445.0 mg, 2.97 mmol), di-tert-butyl 2-chloro-6-(4-(trifluoromethyl)phenylamino)pyrimidin-4yliminodicarbonate (1.0 g, 5.78 mmol), palladium (II) acetate (33.4 mg, 0.149 mmol), triphenylphosphine (46.7 mg, 0.178 mmol), cesium acetate (1.14 g, 5.94 mmol) and DMA (5 mL) was degassed by three cycles of vacuum pumping and N2 purging, and then was heated to 100°C for 1 hour. The solution was cooled and poured into water (50 mL), and this mixture was extracted with dichloromethane. The extract was dried over MgSCU, then filtered and concentrated under the reduced pressure. The residual material was triturated with ethyl ether to afford di-ierZ-butyl 2-(6-fluoro-2-methylimidazo[l,2-«]pyridin-3-yl)-6-(4(trifluoromethyl)phenylamino)pyrimidin-4-yliminodicarbonate (706.0 mg, 83%).
Step 5. A solution of di-tert-butyl 2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-325 yl)-6-(4-(trifluoromethyl)phenylamino)pyrimidin-4-yliminodicarbonate (140 mg, 0.24 mmol)
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PCT/US2013/071132 in dichloromethane (2 mL) was treated with TFA (0.4 mL) at 0°C. The resulting mixture was stirred at ambient temperature for 4 hours. The solvent was concentrated under reduced pressure, and the residual material was partitioned between ethyl acetate and a saturated NaHCOs solution. The organic layer was separated, dried over MgSO4, then filtered and evaporated. The residual material was triturated with ethyl ether to afford the title compound as a white solid (87.0 mg, 87%). m.p. 209-211 °C.
NMR (500 MHz, Acetone-^) δ ppm 10.40 (dd, J= 2.21, 5.36 Hz, 1H), 8.88 (s, 1H), 8.11
- 8.27 (m, 1H), 7.78 - 7.85 (m, 1H), 7.74 (d, J= 8.83 Hz, 2H), 7.69 (d, J= 8.83 Hz, 2H), 6.47 (br. s., 2H), 6.03 (s, 1H), 2.93 (s, 3H); MS m/z 403.5 (100) [M+H]+, 404.4 (30).
Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 5 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
65 N-[4-(difluoromethoxy)phenyl]-2-[2-(trifhioromethyl)imidazo [ 1,2-a]pyridin-3 yl]pyrimidine-4,6-diamine 'H NMR (500 MHz, Acetone-76) δ ppm 9.67 (ddd, 7= 1.10, 1.26, 7.09 Hz, 1H), 8.40 (s, 1H), 7.73 (td, J= 1.10, 9.14 Hz, 1H), 7.59 - 7.66 (d, J = 9.1 Hz, 2H), 7.51 (ddd, 7= 1.26, 6.94, 9.14 Hz, 1H), 7.15 - 7.23 (d, J = 9.1 Hz, 2H), 6.80 - 7.10 (t, J = 75.00 Hz, 1H), 7.05 - 7.12 (m, 1H), 6.11 (br. s., 2H), 5.96 (s, 1H); MS m/z 437.3 [M+H]+
66 2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine m.p. 203-205 °C; MS m/z 439.4 [M+H]+
67 N-[4-(trifluoromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidine-4,6-diamine m.p. 199-202 °C; MS m/z 455.3 [M+H]+
69 N-[4-(difluoromethoxy)phenyl]-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3yl)pyrimidine-4,6-diamine ]H NMR (500 MHz, Acctonc-70) δ ppm 10.41 (dd, 7= 2.21, 5.36 Hz, 1H), 8.57 (s, 1H), 8.19 (s, 1H), 7.71 - 7.89 (m, 1H), 7.53 (d, 7= 9.77 Hz, 2H), 7.20 - 7.26 (d, 7= 9.77 Hz, 2H), 6.81 - 7.11 (t, J = 75.00 Hz, 1H), 6.36 (br, s., 2H), 5.91 (s, 1H), 2.91 (s, 3H); m.p. 136-138 °C; MS m/z 401.5 [M+H]+
75 2-(2-cyclopropyl-6-fluoroimidazo[l,2-a]pyridin-3-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]pyrimidine-4,6-diamine JH NMR (500 MHz, DMSO-76) δ ppm 10.06 (dd, 7= 2.21, 5.99 Hz, 1H), 9.28 (s, 1H), 7.70 - 7.87 (m, 1H), 7.58 (dd, 7= 5.52, 9.62 Hz, 1H), 7.41 (ddd, 7= 2.68, 7.72, 9.77 Hz, 1H), 6.98-7.28 (t, J = 75.00 Hz, 1H), 7.24 - 7.32 (m, 1H), 7.18 - 7.24 (m, 1H), 6.73 (s, 2H), 5.72 (s, 1H), 3.42 - 3.56 (m, 1H), 0.89-1.11 (m, 4H); m.p. 198-200 °C; MS m/z 445.5 [M+H]+
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Cpd Name & Data
84 [3-(4-amino-6-{[4-(trifluoromethyl)phenyl]amino}pyrimidin-2-yl)-6-fluoroimidazo[l,2a]pyridin-2-yl]methanol ’H NMR (500 MHz, METHANOL-i/4) 5 ppm 9.36 - 9.77 (m, 1 H), 7.90 - 7.97 (m, 2 H), 7.59 - 7.69 (m, 1 H), 7.50 - 7.55 (m, 2 H), 7.- 7.45 (m, 1 H), 6.55 - 6.58 (m, 1 H), 4.86 (s, 2 H); MS m/z 419.1 [M+H]+
100 2-(6-fluoro-2-methylimidazo[l,2-a]pyrimidin-3-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 'H NMR (500 MHz, DMSO-t/6) δ ppm 10.45 (dd, J= 2.84, 5.67 Hz, 1H), 9.46 (s, 1H), 8.76 (d, J= 2.84 Hz, 1H), 7.72 (d, J= 8.51 Hz, 2H), 7.64 (d, J= 8.51 Hz, 2H), 6.82 (s, 2H), 5.79 (s, 1H), 2.84 (s, 3H); m.p. 256-258 °C; MS m/z 404.3 [M+H]+
Example 6
2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifhioromethyl)phenyl]pyrimidine-4,6diamine (Cpd 71)
Figure AU2013348009C1_D0159
H2N
Figure AU2013348009C1_D0160
Pd2dba3,
XPhos,
K3PO4, Dioxane
NBoc2
Figure AU2013348009C1_D0161
Figure AU2013348009C1_D0162
Pd/C (10%),
MeOH, EtOAc
Figure AU2013348009C1_D0163
C2H5COOH ACN
EtC(OMe)3
Figure AU2013348009C1_D0164
Step 1: A mixture of 5-fluoro-2-nitroaniline (156.2 mg, 1.00 mmol), ), di-/ert-butyl 2chloro-6-(4-(trifluoromethyl)phenylamino)pyrimidin-4-yliminodicarbonate (480.0 mg, 0.98 mmol), 2-dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl (Xphos) (56.1 mg, 0.1 mmol), tris(dibenzylideneacetone) dipalladium(O) (53.8 mg, 0.05 mmol) and potassium phosphate (625.0 mg, 2.95 mmol) in dioxane (2 mL) was degassed by three cycles of vacuum pumping and N2 purging, and then was heated to 100°C for 2 hours. The solution was cooled and poured into water (10 mL), and this mixture was extracted with ethyl acetate (15 mL). The extract was dried over MgSC>4, then filtered and evaporated. The residual material was
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Step 2: A pressure reaction vessel charged with di-tert-butyl 2-(5-fluoro-2nitrophenylamino)-6-(4-(trifluoromethyl)phenylamino)pyrimidin-4-yliminodicarbonate (483.0 mg), Pd/C (10%, wet, 48.0 mg) and 1:1 ethyl acetate:methanol (5 mL) was placed on a Parr shaker. The mixture was degassed by three cycles of vacuum pumping and N2 purging. The vessel was pressurized to 40 psi hydrogen and shaken for 2 hours. The charcoal was removed by filtration, and the solvent was evaporated to give di-tert-butyl 2-(2-amino-5fhiorophenylamino)-6-(4-(trifhioromethyl)phenylamino)-pyrimidin-4-yliminodicarbonate. The residual material was used in the next step without further purification. MS m/z 579.6 (100) [M+H]+, 580.6(40).
Step 3: A mixture of di-tert-butyl 2-(2-amino-5-fluorophenylamino)-6-(4(trifluoromethyl)-phenylamino)pyrimidin-4-yliminodicarbonate (365.0 mg, 0.63 mmol), triethyl orthoacetate (306.0 mg, 1.89 mmol), p-tolucnesulfonic acid (5.0 mg, 0.025 mmol) and ethanol (2.0 mL) was heated to reflux for 2 hours. After cooling, the mixture was partitioned between di chloromethane (20 mL) and a saturated NaHCCfi solution (10 mL). The organic phase was washed with brine (10 mL), dried over MgSCfi, then filtered and evaporated. The residual oil was triturated with ethyl ether to afford di-tert-butyl 2-(6-fluoro2-methyl-1 H-benzo [i/]imidazol-1 -yl)-6-(4-(trifluoromethyl)phenylamino)pyrimidin-4yliminodicarbonate (316.0 mg, 83%). MS m/z 603.6 (100) [M+H]+, 604.6 (40).
Step 4: A solution of the product (316.0 mg, 0.52 mmol) in dichloromethane (3 mL) was treated with TFA (1 mL) at 0°C. The resulting mixture was stirred at ambient temperature for 4 hours. The solvent was evaporated, and the residual material was triturated with ethyl ether to afford the title compound as a white solid (152.0 mg, 73%). m.p. 253 255°C.
'Η NMR (500 MHz, DMSO-c/rt) δ ppm 9.72 (s, 1H), 8.00 (d, J = 8.51 Hz, 2H), 7.52 - 7.69 (m, 3H), 7.45 (dd, J= 1.89, 9.14 Hz, 1H), 7.01 - 7.24 (m, 3H), 6.20 (s, 1H), 2.66 (s, 3H); MS m/z 403.3 (100) [M+H]+.
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Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 6 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
93 2-(6-chloro-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine ’H NMR (500 MHz, DMSO-r/6) δ ppm 9.76 (s, 1H), 8.19 (d, J = 1.9 Hz, 1H), 7.74 (d, J = 8.5 Hz, 2H), 7.64 (d, J = 8.5 Hz, 2H), 7.60 (d, J = 8.5 Hz, 1H), 7.27 (dd, J = 8.5, 1.9 Hz, 1H), 7.02 (br. s., 2H), 5.90 (s, 1H), 2.83 (s, 3H); MS m/z 419.8 [M+H]+
72 N-[4-(difhioroniethoxy)phenyl]-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine4,6-diamine 'Η NMR (500 MHz, DMSO-4) δ ppm 9.25 (s, 1H), 7.99 (dd, J = 2.21, 10.09 Hz, 1H), 7.56 (dd, J= 5.04, 8.83 Hz, 1H), 7.48 (d, J= 8.83 Hz, 2H), 7.00 - 7.30 (t, J = 75.00 Hz, 1H), 7.12-7.19 (m, 2H), 7.07 (dt, J= 2.36, 9.06 Hz, 1H), 6.84 (br. s., 2H), 5.74 (s, 1H), 2.80 (s, 3H); m.p. 168-170 °C; MS m/z 401.5 [M+H]+
76 N-[4-(difhioromethoxy)-3-fluorophenyl]-2-(6-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine 'fl NMR (500 MHz, DMSO-//rt) δ ppm 9.47 (s, 1H), 7.96 (d, J = 9.14 Hz, 1H), 7.66 (d, J = 12.93 Hz, 1H), 7.57 (dd, J= 5.04, 8.20 Hz, 1H), 7.00 - 7.28 (t, J = 70.00 Hz, 1H), 7.27 7.39 (m, 1H), 7.23 (d, J = 8.51 Hz, 1H), 7.08 (t, J= 8.20 Hz, 1H), 6.94 (br. s., 2H), 5.80 (s, 1H), 2.50 (br. s., 3H); m.p. 182-183 °C; MS m/z 419.4 [M+H]+
77 N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-6-fluoro-1 H-benzimidazol-1yl)pyrimidine-4,6-diamine 'fl NMR (500 MHz, DMSO-^) δ ppm 9.47 (br. s., 1H), 7.90 (d, J= 9.14 Hz, 1H), 7.50 7.74 (m, 2H), 7.29 (d, J= 5.04 Hz, 1H), 7.00 - 7.28 (t, J = 70.00 Hz, 1H), 7.22 (d, 8.20 Hz, 1H), 7.09 (d, J= 7.88 Hz, 1H), 6.93 (br. s., 2H), 5.80 (s, 1H), 3.27 (m,2H), 1.28 (t, J= 6.62 Hz, 3H); m.p. 156-158 °C; MS m/z 433.5 [M+H]+
81 2-(2-ethyl-6-fhioro-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrirnidine-4,6diamine ’H NMR (500 MHz, DMSO-^) δ ppm 9.64 (s, 1H), 7.89 (dd, J = 2.52, 10.09 Hz, 1H), 7.70 (d, J= 8.20 Hz, 2H), 7.58 - 7.66 (m, 3H), 7.05 - 7.13 (m, 1H), 6.98 (br. s., 2H), 5.88 (s, 1H), 3.28 (q, J= 7.46 Hz, 2H), 1.28 (t, 7.57 Hz, 3H); m.p. 201-203 °C; MS m/z 417.2 [M+H]+
96 2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-c/6) δ ppm 9.11 (br. s, 1H), 8.27 (d, J = 2.2 Hz, 1H), 7.78 (dd, J = 13.9, 1.6 Hz, 1H), 7.65 (t, J = 8.5 Hz, 1H), 7.56 (d, J == 8.5 Hz, 1H), 7.49 (d, J = 8.8 Hz, 1H), 7.25 (dd, J == 8.5, 1.9 Hz, 1H), 6.57 (br. s., 2H), 6.07 (s, 1H), 2.87 (s, 3H); MS m/z 437.8 [M+H]+
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Cpd Name & Data
97 2-(6-chloro-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine4,6-diamine ]H NMR (500 MHz, Acetone-c/g) δ ppm 8.56 (br. s, 1H), 8.32 (d, J = 2.2 Hz, 1H), 7.56 (dd, J = 6.6, 2.2 Hz, 2H), 7.53 (d, J = 8.8 Hz, 1H), 7.23 (dd, J = 8.5, 2.2 Hz, 1H), 7.20 (dd, J = 6.6, 2.2 Hz, 2H), 6.94 (t, J = 74.7 Hz, 1H), 6.35 (br. s„ 2H), 5.91 (s, 1H), 2.85 (s, 3H); MS m/z 418.0 [M+H]+
98 2-(5-chloro-2-methyl-l H-benzimidazol-l-yl)-N-[3-fluoro-4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine ’H NMR (500 MHz, DMSO-TO δ ppm 9.94 (br. s, 1H), 8.10 (d, J = 8.7 Hz, 1H), 7.82 (dd, J = 14.3, 1.4 Hz, 1H), 7.67 (d, J = 2.0 Hz, 1H), 7.65 (d, J = 8.7 Hz, 1H), 7.42 (dd, J = 8.7, 1.1 Hz, 1H), 7.27 (dd, J = 8.7, 2.0 Hz, 1H), 7.10 (br. s, 2H), 5.93 (s, 1H), 2.83 (s, 3H); MS m/z 437.8 [M+H]+
99 2-(5-chloro-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine4,6-diamine Ή NMR (500 MHz, DMSO-76) δ ppm 8.99 (br. s, 1H), 8.72 (d, J = 8.8 Hz, 1H), 8.03 (d, J = 2.5 Hz, 1H), 8.00 - 8.03 (m, 2H), 7.65 - 7.67 (m, 2H), 7.64 (dd, J = 8.8, 2.2 Hz, 1H), 7.42 (t, J = 75.0 Hz, 1H), 6.79 (br. s., 2H), 6.38 (s, 1H), 3.32 (s, 3H); MS m/z 417.8 [M+H]+
144 N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)pyrimidine-4,6diamine *H NMR (500 MHz, DMSO-riQ δ ppm 9.25 (s, 1H), 7.84 - 8.12 (m, 1H), 7.60 (dd, J = 5.04, 8.51 Hz, 1H), 7.49 (d, J= 8.83 Hz, 2H), 7.01 - 7.31 (t, J = 75.00 Hz, 1H), 7.15 (d, J = 8.20 Hz, 2H), 7.04 - 7.13 (m, 1H), 6.84 (br. s., 2H), 5.76 (s, 1H), 3.28 (q, J= 7.25 Hz, 2H), 1.28 (t, 7=7.41 Hz,3H);m.p. 166-168 °C; MS m/z 415.4 [M+H]+
Example 7
2-(2-cyclopropyl-6-fluoro-1H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine (Cpd 82)
Figure AU2013348009C1_D0165
Figure AU2013348009C1_D0166
Figure AU2013348009C1_D0167
Step 1: To a solution of di-tert-butyl 2-(2-amino-5-fluorophenylamino)-6-(4(trifluoromethyl)-phenylamino)pyrimidin-4-yliminodicarbonate (212.0 mg, 0.37 mmol), triethylamine (42.0 mg, 0.41 mmol) in dichloromethane (2 mL) was added cyclopropanecarbonyl chloride (38.3 mg, 0.37 mmol) at 0°C. The mixture was stirred at ambient temperature for 3 hours, then partitioned between dichloromethane and water. The
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Step 2: A mixture of crude di-terLbutyl 2-(2-(cyclopropanecarboxamido)-5fluorophenylamino)-6-(4-(trifluoromethyl)phenylamino)-pyrimidin-4-yliminodicarbonate, p-toluenesulfonic acid (7.0 mg, 0.037 mmol) and acetonitrile (3 mL) was heated in a microwave oven at 180°C for 30 minutes. The mixture was partitioned between ethyl acetate and a saturated NaHCCh solution. The organic phase was washed with brine, dried over MgSO4, then filtered and evaporated. The residual material was separated by silica gel column chromatography (eluting with 1:1 dichloromethane.’hexane, then 1:5 MeOH:50% ethyl acetate in dichloromethane) to afford the title compound (103.0mg, 65% for two steps), m.p. 203 - 206°C.
*H NMR (500 MHz, DMSO-ri6) δ ppm 9.49 - 9,59 (m, 1H), 7.70 (td, 7 = 1.00, 13.24 Hz, 1H), 7.64 (d, J= 8.57 Hz, 2H), 7.49 (d, 7 = 8.57 Hz, 2H), 7.36 - 7.42 (m, 1H), 6.91 - 6.97 (m, 1H), 6.88 (br. s, 2H), 5.77 (s, 1H), 2.88 - 3.01 (m, 1H), 0.97 - 1.05 (m, 2H), 0.86 - 0.95 (m, 2H); MS m/z 429.2 (100) [M+H]+, 430.2 (20).
Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 7 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
78 2-(2-cyclopropyl-6-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]pyrimidine-4,6-diarnine ’H NMR (500 MHz, DMSO-76) δ ppm 9.53 (s, 1H), 7.70 - 7.95 (m, 2H), 7.52 (dd,7 = 5.04, 8.83 Hz, 1H), 7.28 (d, J= 2.52 Hz, 1H), 6.98 - 7.26 (t, J = 70.00 Hz, 1H), 7.22 (m, 1H), 7.03 - 7.09 (m, 1H), 6.98 (br. s, 2H), 5.82 (s, 1H), 3.07 (m, 1H), 1.10 - 1.15 (m, 2H), 1.01 - 1.08 (m, 2H); m.p. 186-188 °C; MS m/z 445.5 [M+H]+
83 2-(2-cyclopropyl-5-fluoro-1 H-benzimidazol-1 -yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, DMSO-7rt) δ ppm 9.69 (s, 1H), 7.96 (d, J= 5.04, 8.83 Hz, 1H), 7.79 (d, J = 8.51 Hz, 2H), 7.61 (d, J= 8.51 Hz, 2H), 7.34 (dd, J= 2.52, 9.46 Hz, 1H), 6.93 7.09 (m, 3H), 5.78 - 5.93 (m, 1H), 3.02 (s, 1H), 1.13 - 1.19 (m, 2H), 1.04 - 1.08 (m, 2H); MS m/z 6192 [M+H]+
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Cpd Name & Data
143 2-(2-cyclopropyl-6-fluoro-1 H-benzimidazol-1 -yl)-N- [4(difluoromethoxy)phenyl]pyrimidine-4,6-diamine ’H NMR (500 MHz, DMSO-iZ6) δ ppm 9.30 (s, 1H), 7.83 - 7.90 (m, 1H), 7.54 (d, J= 8.83 Hz, 3H), 7.00 - 7.30 (t, J = 75.00 Hz, 1H), 7.11 - 7.18 (m, 2H), 7.02 - 7.10 (m, 1H), 6.83 6.92 (m, 2H), 5.78 (s, 1H), 3.08 - 3.20 (m, 1H), 1.09 - 1.14 (m, 2H), 0.99 - 1.07 (m, 2H); m.p. 175-177 °C; MS m/z 427.2 [M+H]+
145 N-[4-(difluoromethoxy)phenyl]-2-[2-(difluoromethyl)-6-fluoro-lH-benzimidazol-lyl]pyrimidine-4,6-diamine !H NMR (500 MHz, DMSO-JQ δ ppm 9.32 (s, 1H), 8.36 (dd, 1.89, 10.09 Hz, 1H), 7.95 - 8.16 (t, J = 52.5 Hz, 1H), 7.85 (dd, J= 5.04, 8.83 Hz, 1H), 7.44 (d, J= 8.83 Hz, 2H), 7.04 - 7.34 (t, J = 75.00 Hz, 1H), 7.27 (dt, 2.36, 9.06 Hz, 1H), 7.20 (d, J = 8.83 Hz, 2H), 6.98 (br. s„ 2H), 5.76 (s, 1H); m.p. 114-115 °C; MS m/z 437.4 [M+H]+
149 2-(2-cyclopropyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine JH NMR (500 MHz, DMSO-4) δ ppm 9.70 (s, 1H), 7.92 - 7.97 (m, 1H), 7.81 (d, J= 8.51 Hz, 2H), 7.60 (d, J= 8.51 Hz, 2H), 7.50 - 7.55 (m, 1H), 7.19 (ddd, J= 1.58, 5.04, 7.25 Hz, 2H), 7.00 (br. s., 2H), 5.90 (s, 1H), 2.94 - 3.03 (m, 1H), 1.15 (m, 2H), 1.05 (m, 2H); m.p. 199-201 °C; MS m/z 411.3 [M+H]+
150 2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine JH NMR (500 MHz, DMSO-J6) δ ppm 9.66 (s, 1H), 8.09 - 8.20 (m, 1H), 7.73 (d, J = 8.51 Hz, 2H), 7.67 - 7.71 (m, 1H), 7.63 (d, J= 8.51 Hz, 2H), 7.26 - 7.31 (m, 2H), 6.97 (br. s., 2H), 5.87 (s, 1H), 5.04 (s, 2H), 3.25 (s, 3H); m.p. 212-213 °C; MS m/z 415.4 [M+H]+
151 2-[2-(propan-2-yl)-1 H-benzimidazol-1 -yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine 'bl NMR (500 MHz, DMSO-^) δ ppm 9.69 (s, 1H), 7.85 - 7.91 (m, 1H), 7.74 (d, J= 8.83 Hz, 2H), 7.61 - 7.65 (m, 1H), 7.59 (d, J= 8.83 Hz, 2H), 7.17 - 7.25 (m, 2H), 6.95 (s, 2H), 5.90 (s, 1H), 3.96 - 4.08 (m, 1H), 1.29 (d, 6.94 Hz, 6H); m.p. 216-218 °C; MS m/z 413.4 [M+H]+
152 2-[2-(difluoromethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine 'H NMR (500 MHz, DMSO-O δ ppm 9.71 (s, 1H), 8.36 - 8.52 (m, 1H), 7.89 - 8.11 (t, J = 55.00 Hz, 1H), 7.80 - 7.87 (m, 1H), 7.68 (m. 4H), 7.35 - 7.48 (m, 2H), 6.92 - 7.20 (m, 2H), 5.91 (s, 1H); m.p. 187-188 °C; MS m/z 421.4 [M+H]+
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Example 8
2-(6-fluoro-2-m ethyl-1 H-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6-diamine (Cpd 265)
Figure AU2013348009C1_D0168
Figure AU2013348009C1_D0169
Step 1: To a mixture of 5-fluoro-2-nitroaniline (8.16 g, 35.93 mmol), 4,6-dichloro-2(methylsulfonyl)pyrirnidine (5.06 g, 32.67 mmol), THF (50 mL) and DMF (12 mL) was added sodium terripentoxide (2.5 M in THF, 28.6mL, 71.5 mmol) dropwise at -78°C. The mixture was stirred at -78°G for 30 minutes, then ice/water (300 mL) was added to form a precipitate. The solid was collected by filtration, then washed with water and hexane to afford 4,6-dichloro-N-(5-fluoro-2-nitrophenyl)pyrimidin-2-amine (9.32 g, 95%).
Step 2: A 250 mL flask charged with 4,6-dichloro-N-(5-fluoro-2nitrophenyI)pyrimidin-2-amine (6.35 g, 21.03 mmol), Pd/C (10%, wet, 635.0 mg) and ethyl acetate (50 mL) was degassed by three cycles of vacuum pumping and N2 purging, and then filled with hydrogen from a hydrogen balloon. The mixture was stirred at ambient temperature for 16 hours. The charcoal was removed by filtration, and the solvent was evaporated. The residual material was washed with hexane to afford N1 -(4,6dichloropyrimidin-2-yl)-5-fluorobenzene-l,2-diamine as a white solid (5.55 g, 97%).
Step 3: A mixture of N1-(4,6-dichloropyrimidin-2-yl)-5-fluorobenzene-l,2-diamine (2.57 g, 9.47 mmol), triethyl orthoacetate (6.06 g, 37.87 mmol), acetic acid (6 mL) and acetonitrile (30 mL) was stirred at ambient temperature for 18 hours. A saturated NaHCO3 solution was added to the mixture portionwise at 0°C, with resultant bubbling of the mixture.
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The solution was added to the mixture until the bubbling ceased. The product was then extracted with ethyl acetate. The organic phase was washed with brine, dried over MgSCL, then filtered and evaporated. The residual material was washed with hexane to afford 1 -(4,6dichloropyrimidin-2-yl)-6-fluoro-2-methyl-lH-benzo[d]imidazole as a brownish solid (2.41 g, 86%).
Step 4: A mixture of 1-(4,6-dichloropyrimidin-2-yl)-6-fluoro-2-methyl-lHbenzo[d]imidazole (150.0 mg, 0.51 mmol), 4-methoxyaniline (125.0 mg, 1.01 mmol) and acetonitrile (1 mL) was stirred at 80°C for 18 hours. After cooling, ethyl ether was added to the mixture to form 6-chloro-2-(6-fhioro-2-methyl-lH-benzo[d]imidazol-l-yl)-N-(4methoxyphenyl)pyrimidin-4-amine as a precipitate, which was isolated by filtration.
Step 5: To 6-chloro-2-(6-fhioro-2-methyl-lH-benzo[d]imidazol-l-yl)-N-(4methoxyphenyl)-pyrimidin-4-amine was added DMSO (2 mL) and NH4OH (27%, 0.1 mL). The reaction mixture was sealed, placed in a microwave oven and heated at 170°C for 1 hour. The reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with water (2 x 20 mL) and brine, then dried over MgSCU and filtered through a silica gel pad (10 g). The solvent was evaporated, and the residual material was triturated with dichloromethane to afford the title compound as a white solid (161.0 mg, 88%). m.p. 193 - 195°C.
’H NMR (500 MHz, Acetone-ri6)D δ ppm 8.74 (s, 1H), 8.11 (dd, J= 2.52,10.40 Hz, 1H), 7.52 (dd, 5.20, 8.67 Hz, 1H), 7.34 - 7.43 (d, J= 9.14 Hz, 2H), 7.01 (d, J= 2.84 Hz, 1H), 6.94 (d, J= 9.14 Hz, 2H), 6.49 (br. s„ 2H), 5.76 (s, 1H), 3.79 (s, 3H), 2.84 (s, 3H); MS m/z 365.0 (100) [M+H]‘ .
Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 8 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
52 2- {[6- {[4-(difluoromethoxy)phenyl] amino } -2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin4-yl] amino } ethanol *H NMR (500 MHz, Methanol-^) δ ppm 8.17 (1H, dd, J = 7.2, 1.5 Hz), 7.59 (1H, dd, J = 7.2, 1.5 Hz), 7.51 (2H, d, J = 9 Hz), 7.28 (1H, m), 7.13 (2H, d, J = 9 Hz), 6.78 (1H, t, J = 75 Hz), 5.81 (1H, s), 3.75 (2H, t, J = 6 Hz), 3.53 (2H, br), 2.89 (3H, s); MS m/z 427.1 [M+H]+
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Cpd Name & Data
57 2-( [2-(2-methyl-1 H-benzimidazol-1 -yl)-6- {[4-(trifluoromethyl)phenyl] amino} pyrimidin4-yl] amino } ethanol *H NMR (500 MHz, Methanol-^) δ ppm 8.13 (1H, d, J = 7.5 Hz), 7.71 (2H, d, J = 7.5 Hz), 7.6 (1H, dd, J = 9, 1 Hz), 7.56 (2H, d, J = 9 Hz), 7.27 (1H, m), 7.13 (2H, d, J = 9 Hz), 5.91 (1H, s), 3.76 (2H, t, J = 6 Hz), 3.55 (2H, br), 2.89 (3H, s); MS m/z 429.2 [M+H]+
58 N4-(2-methoxyethyl)-2-(2-methyl-1 H-benzimidazol-1 -yl)-N6- [4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 1H NMR (Methanol-i/4) δ ppm 8.15 (1H, d, J = 8 Hz), 7.67 (2H, d, J =8.5 Hz), 7.59 (1H, d, J = 8 Hz), 7.53 (2H, d, J = 8.5 Hz), 7.26 (1H, m), 5.87 (1H, s), 3.58 (4H, br), 3.38 (3H, s).2.87 (3H, s); MS m/z 443.1 [M+H]+
59 N4-[4-(difluoromethoxy)phenyl]-N6-(2-methoxyethyl)-2-(2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine 'H NMR (500 MHz, Methanol-tZ4) δ ppm 8.06 (1H, d, J = 7 Hz), 7.47 (1H, m), 7.38 (2H, d, J = 9 Hz), 7.15 (1H, m), 7.00 (2H, d, J = 9 Hz), 5.68 (1H, s), 3.28 (3H, s), 2.76 (3H, s); MS m/z 441.1 [M+H]+
63 2-(2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine ]H NMR (500 MHz, Methanol-iZ4) δ ppm 8.13 (1H, m), 7.73 (2H, d, J = 8.5 Hz), 7.61 (1H, m), 7.58 (2H, d, J = 8.5 Hz), 7.29 (2H, m), 5.95 (1H, s), 2.89 (3H, s); MS m/z 385.1 [M+H]+
64 2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 'll NMR (500 MHz, Methanol-0/4) δ ppm 8.19 (1H, dd, J = 11, 7.5 Hz), 7.67 (2H, d, J = 8.5 Hz), 7.6 (2H, d, J = 8.5 Hz), 7.43 (1H, dd, J = 11, 7.5 Hz), 5.93 (1H, s), 2.9 (3H, s); MS m/z 421.1 [M+H]+
73 2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine ’H NMR (500 MHz, Methanol-^) δ ppm 8.61 (1H, dd, J = 8, 1.5 Hz), 8.39 (1H, d, J = 4 Hz), 7.65 (2H, d, J = 8.5 Hz), 7.57 (2H, d, J = 8.5 Hz), 7.28 (1H, dd, J = 8, 4 Hz), 5.91 (1H, s), 2.97 (3H, s); MS m/z 386.2 [M+H]+
74 2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4- (trifluoromethyl)phenyl]pyrimidine-4,6-diamine 'H NMR (500 MHz, Methanol-ri4) δ ppm 8.04 (1H, dd, J = 11, 7.5 Hz), 7.54 (1H, dd, J = 13.5, 1.5 Hz), 7.44 (1H, t, J = 8.5 Hz), 7.32 (1H, dd, J = 11, 7.5 Hz), 7.24 (1H, dd, J = 13.5, 1.5 Hz), 5.81 (1H, s), 2.78 (3H, s); MS m/z 439.1 [M+H]+
79 N-[4-(trifluoromethyl)phenyl]-2-(2,5,6-trimethyl-lH-benzimidazol-l-yl)pyrimidine-4,6di amine ’H NMR (500 MHz, DMSO-J6) δ ppm 9.63 (s, 1H), 7.91 (s, 1H), 7.77 (d(AB), J = 8.8 Hz, 2H), 7.63 (d(AB), J = 7.9 Hz, 2H), 7.34 (s, 1H), 6.92 (br. s., 2H), 5.85 (s, 1H), 2.79 (s, 3H), 2.31 (s, 3H), 2.26 (s, 3H); MS m/z 413.0 [M+H]+
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Cpd Name & Data
80 N-[3-fluoro-4-(trifluoromethyl)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine4,6-diamine ’ll NMR (500 MHz, DMSO-^) δ ppm 9.90 (s, 1H), 8.05 - 8.10 (m, 1H), 7.89 (d, J = 14.2 Hz, 1H), 7.65 (t, J = 8.7 Hz, 1H), 7.57 - 7.62 (m, 1H), 7.41 (d, J = 8.5 Hz, 1H), 7.20 - 7.28 (m, 2H), 7.05 (br. s, 1H), 5.91 (s, 1H), 2.82 (s, 3H); MS m/z 403.1 [M+H]+
85 2-(6-bromo-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine JH NMR (500 MHz, DMSO-</6) δ ppm 9.68 (s, 1H), 8.31 (d, J = 1.6 Hz, 1H), 7.73 (d(AB), J = 8.2 Hz, 2H), 7.65 (d(AB), J = 8.5 Hz, 2H), 7.55 (d, J = 8.5 Hz, 1H), 7.39 (dd, J = 8.5, 1.9 Hz, 1H), 6.97 - 7.07 (m, 2H), 5.87 (s, 1H), 2.83 (s, 3H); MS m/z 463.0 [M+H]+
86 2-(2,6-dimethyl-lH-benzimidazol-l-yl)-N-[4-(trifluorornethyl)phenyl]pyrimidine-4,6diamine ’H NMR (500 MHz, DMSO-J6) δ ppm 9.63 (s, 1H), 7.88 (s, 1H), 7.74 (d(AB), J = 8.5 Hz, 2H), 7.61 (d(AB), J = 8.5 Hz, 2H), 7.44 (d, J = 8.2 Hz, 1H), 7.04 (dd, J = 8.2, 1.3 Hz, 1H), 6.93 (br. s., 2H), 5.84 (s, 1H), 2.77 (s, 3H), 2.34 (s, 3H); MS m/z 339.0 [M+H]+
87 2-(6-ethyl-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine *H NMR (500 MHz, DMSO-r/Q δ ppm 9.68 (s, 1H), 7.89 (s, 1H), 7.77 (d(AB), J = 8.5 Hz, 2H), 7.61 (d(AB), J = 8.8 Hz, 2H), 7.52 (d, J = 8.2 Hz, 1H), 7.10 (dd, J = 8.2, 1.3 Hz, 1H), 6.95 (br. s., 2H), 5.86 (s, 1H), 2.81 (s, 3H), 2.64 (q, J = 7.6 Hz, 2H), 1.15 (t, J = 7.6 Hz, 3H); MS m/z 413.0 [M+H]+
88 2-(4,6-difluoro-2-methyl-1 H-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 1H NMR (500 MHz, DMSO-JQ δ ppm 9.68 (s, 1H), 7.85 (dd, J = 9.6, 2.0 Hz, 1H), 7.68 - 7.73 (d(AB), J = 8.5 Hz, 2H), 7.61 - 7.68 (d(AB), J = 8.8 Hz, 2H), 7.14 (td, J = 10.4, 2.2 Hz, 1H), 7.04 (br. s., 2H), 5.89 (s, 1H), 2.83 (s, 3H); MS m/z 421 [M+H]+
89 2-(4,6-difluoro-2-methyl-lH-benzimidazol-1-yl)-N-[3-fluoro-4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 'Η NMR (500 MHz, DMSO-^) δ ppm 9.92 (s, 1H), 7.80 - 7.84 (m, J = 9.5, 2.2 Hz, 1H), 7.80 (dd, J = 14.0, 1.1 Hz, 1H), 7.66 (t, J = 8.7 Hz, 1H), 7.38 (dd, J = 8.5, 1.3 Hz, 1H), 7.16 (dd, J = 10.4, 2.2 Hz, 1H), 7.11 -7.16(m, 2H), 5.91 (s, 1H); MS m/z 439 [M+H]+
90 2- {[2-(4,6-difluoro-2-methyI-1 H-benzimidazol-1 -yl)-6- {[4(trifluoromethyl)phenyl]amino}pyrimidin-4-yl]amino} ethanol ‘H NMR (500 MHz, DMSO-ί/,ί) δ ppm 9.69 (br. s., 1H), 7.83 (d, J = 9.1 Hz, 1H), 7.70 (d(AB), J = 7.9 Hz, 2H), 7.64 (d(AB), J = 8.8 Hz, 2H), 7.15 (td, J = 10.3, 2.4 Hz, 1H), 5.96 (br. s, 1H), 4.83 (br. s, 1H), 3.59 (q, J = 5.7 Hz, 2H), 3.38 - 3.51 (m, 2H), 2.85 (s, 3H); MS m/z 465.0 [M+H]+
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Cpd Name & Data
91 2-(6-ethenyl-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine !H NMR (500 MHz, DMSO-7rt) δ ppm 9.68 (s, 1H), 8.17 (d, J = 1.6 Hz, 1H), 7.76 (d, J = 8.5 Hz, 1H), 7.61 (d, J = 8.8 Hz, 1H), 7.54 (d, J = 8.2 Hz, 1H), 7.39 (dd, J = 8.4,1.4 Hz, 1H), 6.98 (br. s., 1H), 6.75 (dd, J = 17.7, 11.0 Hz, 1H), 5.87 (s, 1H), 5.64 (dd, J = 17.7, 0.6 Hz, 1H), 5.13 (dd, J = 11.0, 0.9 Hz, 1H), 2.82 (s, 1H); MS m/z 399 [M+H]+
92 2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridm-l-yl)-N-[4(trifluoromethyI)phenyl]pyrimidine-4,6-diamine 'Η NMR (500 MHz, Methanol-^) δ ppm 8.37 (1H, dd, J = 9, 3 Hz), 8.3 (1H, m), 7.72 (2H, d, J = 8.5 Hz), 7.6 (2H, d, J = 8.5 Hz), 5.96 (1H, s), 1.33 (2H, m), 1.19 (2H, m); MS m/z 430.1 [M+H]+
94 2-(6-fluoro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4- (trifluoromethyl)phenyl]pyrimidine-4,6-diamine JH NMR (500 MHz, Methanol-^) δ ppm 8.52 (1H, dd, J = 9, 3 Hz), 8.33 (1H, dd, m), 7.65 (2H, d, J = 9 Hz), 7.60 (2H, d, J = 9 Hz), 5.95 (1H, s), 3.00 (3H, s); MS m/z 404.2 [M+H]+
101 N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(5,6-difluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine ’H NMR (500 MHz, Methanol-^) δ ppm 8.19 (1H, dd, J = 11, 7.5 Hz), 7.53 (1H, dd, J = 13, 2.5 Hz), 7.44 (1H, dd, J = 10, 7.5 Hz), 7.23 (2H, m), 5.86 (1H, s), 2.89 (3H, s); MS m/z 437.1 [M+H]+
102 N-[4-(difluoromethoxy)phenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine 'tl NMR (Methanol-^) δ ppm 8.18 (1H, dd, J = 11.5, 7.5 Hz), 7.44 (2H, d, J = 9 Hz), 7.40 (1H, dd, J = 11.5, 7.5 Hz), 7.14 (2H, d, 9 Hz), 6.77 (1H, t, J = 75 Hz), 5.79 (1H, s), 2.87 (lH, s); MS m/z 419.1 [M+H]+
103 2-(2-cyclopropyl-6-fluoro-1 H-imidazo[4,5-b]pyridin-1-yl)-N-[4(difluoromethoxy)phenyl]pyrimidine-4,6-diamine ’ll NMR (500 MHz, Methanol-74) δ ppm 8.38 (1H, dd, J = 9, 3 Hz), 8.29 (1H, m), 7.5 (2H, d, J = 9 Hz), 7.14 (2H, d, J = 7 Hz), 6.78 (1H, t, J = 75 Hz), 3.4 (1H, m), 1.3 (2H, m), 1.17 (2H, m); MS m/z 428.1 [M+H]+
104 2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4- (trifluoromethyl)phenyl]pyrimidine-4,6-diamine ’H NMR (500 MHz, METH ANOL-74) δ ppm 8.77 (d, 7=2.21 Hz, 1H), 8,43 (d, 7=2.21 Hz, 1H), 7.60 (d, 7=6.94 Hz, 4H), 5.91 (s, 1H) 3.05 (s, 3H); MS m/z 420.1 [M+H]+
105 2-(6-chloro-2-ethyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, METHANOL-74) δ ppm 8.66 (d, 7=2.52 Hz, 1H), 8.38 (d, 7=2.21 Hz, 1H), 7.62 (dd, 7=19.50, 9.50 Hz, 4H), 5.92 (s, 1H), 3.48 (q, 7=7.60 Hz, 2H), 1.39 (t, 7=7.41 Hz, 3H); MS m/z 434.1 [M+H]+
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Cpd Name & Data
146 2-(2-methyl-1 H-benzimidazol- l-yl)-N-[4-(methylsulfanyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-74) δ ppm 8.45 - 8.50 (1H, s) 8.25 - 8.30 (1H, m) 7.55 7.59 (1H, m) 7.50 (2H, s) 7.32 (2H, s) 7.17 - 7.25 (2H, m) 6.24 - 6.33 (2H, m) 5.92 (1H, s) 2.51 (3H, s) 2.07 (3H, s); MS m/z 363.2 [M+H]+
147 2-[2-(l-methylcyclopropyl)-lH-benzimidazol-l-yl]-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 'll NMR (500 MHz, Acetone-d^) δ ppm 8.72 - 8.80 (1H, s) 7.66 - 7.76 (3H, m) 7.46 (3H, d, 7=0.63 Hz) 7.08 (2 H, s) 6.18 - 6.28 (2H, m) 5.97 (lH,s) 1.30 (3H, s) 1.10 (2H, s) 0.61 (2H, d, 7=2.21 Hz); MS m/z 425.2 [M+H]+
148 N-[4-(difluoromethoxy)phenyl]-2-[2-( 1 -methyl cyclopropyl)-1 H-benzimidazol-1 yl]pyrimidine-4,6-diamine ’Η NMR (500 MHz, Acetone-7^) δ Dppm 8.49 (1H, s) 8.16 - 8.20 (1H, m) 7.55 - 7.60 (3H, m) 7.15 - 7.23 (4H, m) 6.94 (1H, t, 7=75.00 Hz) 6.27 (2H, br. s.) 5.92 (1H, s) 3.32 (2H, q, 7=7.57 Hz) 1.34 (3H, t, 7=6.90 Hz); MS m/z 423.3 [M+H]+
153 2-(2-ethyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine ’H NMR (500 MHz, DMSO-76) δ ppm 9.66 (s, 1H), 7.96 - 8.10 (m, 1H), 7.73 (d, 7= 8.83 Hz, 2H), 7.58 - 7.64 (m, 3H), 7.18 - 7.26 (m, 2H), 6.96 (br. s, 2H), 5.88 (s, 1H), 3.22 - 3.29 (m, 2H), 1.29 (t, J= 7.41 Hz, 3H); m.p. 183-185 ; MS m/z 415.4 (100) [M+H]+, 416.4 (30)
156 N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6-diamine 'H NMR (500 MHz, Acetonc-7;) δ ppm 8.49 (1H, s) 8.16 - 8.20 (1H, m) 7.55 - 7.60 (3H, m) 7.15 - 7.23 (4H, m) 6.94 (1H, t, 7=75.00 Hz) 6.27 (2H, br. s.) 5.92 (1H, s) 3.32 (2H, q, 7=7.57 Hz) 1.34 (3H, t, 7=6.90 Hz); MS m/z 397.2 [M+H]+
157 N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine NMR (500 MHz, Acetone-d6) δ ppm 8.71 (1H, s) 8.13 - 8.18 (1H, m) 7.68 - 7.75 (1H, m) 7.57 - 7.62 (1H, m) 7.26 - 7.35 (2H, m) 7.16 - 7.25 (2H, m) 6.94 (1H, t, 7=73.80 Hz) 6.36 (2H, s) 5.98 (1H, s) 3.33 (2H, q, 7=7.60 Hz) 1.35 (3H, t, 7=7.90 Hz); MS m/z 415.2 [M+H]+
182 2-[2-(methylsulfanyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine 'H NMR (500 MHz, Acetone-^) δ ppm 8.85 (br. s., 1H) 8.38 (d, 7=7.88 Hz, 1H), 7.83 (d, 7=8.51 Hz, 2H), 7.66 (d, 7=8.51 Hz, 2H), 7.56 (d, 7=7.57 Hz, 1H), 7.23 (td, 7=7.57, 1.26 Hz, 1H), 7.13 - 7.19 (m, 1H), 6.41 (br. s., 2H), 6.02 (s, 1H), 2.63 (s, 3 H); MS m/z 418.3 [M+H]+
196 2-(2-methyl-l H-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine JH NMR (500 MHz, Methanol-74) δ ppm 8.13 (1H, m), 7.58 (1H, m), 7.3-7.25 (4H, m), 7.13 (1H, d, J = 8 Hz), 5.81 (1H, s), 2.86 (3H, s), 2.31 (3H, s); MS m/z 331.1 [M+H]+
197 N-(4-methoxyphenyl)-2-(2-m ethyl-1 H-benzimidazol-l-yl)pyrimidine-4,6-diamine 'H NMR (500 MHz, Methanol-d4) δ ppm 8.13 (1H, m), 7.58 (1H, m), 7.33 (2H, d, J = 9 Hz), 7.27 (2H, m), 6.94 (2H, d, J = 9 Hz), 5.72 (1H, s), 3.81 (3H, s), 2.86 (3H, s); MS m/z 347.1 [M+H]+
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Cpd Name & Data
198 N-[4-(dimethylamino)phenyl]-2-(2 -methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6-diamine ]H NMR (500 MHz, Methanol-^) δ ppm 8.12 (1H, m), 7.58 (1H, m), 7.27 (2H, m), 7.22 (2H, d, J = 9 Hz), 6.81 (2H, d, J = 9 Hz), 5.67 (1H, s), 2.92 (6H, s), 2.86 (3H, s); MS m/z 360.4 [M+H]+
205 N-(l,3-benzodioxol-5-yl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine *H NMR (500 MHz, DMSO-rirt): δ ppm 9.04 (1H, s), 8.20-8.17 (1H, m), 7.61-7.58 (1H, m), 7.27-7.21 (2H, m), 7.15 (1H, d, J = 1.8 Hz), 6.91 (1H, d, J = 8.2 Hz), 6.86 (1H, dd, J = 8.2, 1.8 Hz), 6.76 (2H, br s), 6.03 (2H, s), 5.72 (1H, s), 2.84 (3H, s); m.p. 166-167; MS m/z 359.1 [M+H]+
206 N-(2,2-difluoro-l,3-benzodioxol-5-yl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6di amine *H NMR (500 MHz, DMSO-drt): δ ppm 9.40 (1H, s), 8.13 (1H, dd, J = 7.0, 1.2 Hz), 7.71 (1H, d, J = 2.1 Hz), 7.61 (1H, dd, J = 7.0, 1.2 Hz), 7.38 (1H, d, J = 8.6 Hz), 7.28-7.20 (3H, m), 6.88 (2H, br s), 5.79 (1H, s), 2.83 (3H, s); m.p.: 141-142; MS m/z 397.1 [M+H]+
207 N-(3 -fluoro-4-methoxyphenyl)-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6diamine *H NMR (500 MHz, DMSO-rZ6): δ ppm 9.19 (1H, s), 8.18-8.15 (1H, m), 7.62-7.59 (1H, m), 7.50 (1H, dd, J = 13.6, 2.2 Hz), 7.28-7.13 (4H, m), 6.82 (2H, br s), 5.76 (1H, s), 3.85 (3H, s), 2.84 (3H, s); m.p.: 233-234; MS m/z 365.2 [M+H]+
208 N-(6-methoxypyridin-3-yl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine JH NMR (500 MHz, DMSO-i4): δ ppm 9.10 (1H, s), 8.24 (1H, d, J = 2.6 Hz), 8.14 (1H, dd, J = 8.4, 1.2 Hz), 7.84 (1H, dd, J = 8.8, 2.7 Hz), 7.59 (1H, dd, J = 8.4, 1.5 Hz), 7.277.20 (2H, m), 6.85 (1H, d, J = 8.8 Hz), 6.80 (2H, br s), 5.69 (1H, s), 3.87 (3H, s), 2.80 (3H, s); m.p.: 11.8-119; MS m/z 348.2 [M+H]+
209 N-(4-chlorophenyl)-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6-diamine ’H NMR (500 MHz, Methanol-^) δ ppm 8.11 (1H, m), 7.58 (1H, m), 7.45 (2H, d, J = 9 Hz), 7.28-7.23 (4H, m), 5.83 (1H, s), 2.85 (3H, s); MS m/z 351.6 [M+H]+
210 4- {[ 6-amino-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-yl] amino}benzonitrile ’H NMR (500 MHz, Methanol®) δ ppm 8.1 (1H, m), 7.75 (2H, d, J = 9 Hz), 7.61 (3H, m), 7.28 (2H, m), 5.95 (1H, s), 2.88 (3H, s); MS m/z 342.3 [M+H]+
211 2-(2-methyl-lH-benzimidazol-l-yl)-N-(4-nitrophenyl)pyrimidine-4,6-diamine ’H NMR (500 MHz, Methanol-^) δ ppm 8.16 (2H, m), 8.12 (1H, m), 7.79 (2H, m), 7.62 (1H, m), 7.29 (2H, m), 5.99 (1H, s), 2.90 (3H, s); MS m/z 362.3 [M+H]+
212 N-(4-bromophenyl)-2-(2-methyl-1 H-benzimidazol- l-yl)pyrimidine-4,6-diamine JH NMR (500 MHz, Methanol-^) δ ppm 8.11 (1H, m), 7.59 (1H, m), 7.42 (4H, m), 7.27 (2H, m), 5.84 (1H, s), 2.86 (3H, s); MS m/z 397.0 [M+H]+
221 2-(2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6diamine ’Η NMR (500 MHz, Methanol®) δ ppm 8.11 (1H, m), 7.57 (1H, m), 7.54 (2H, d, 9 Hz), 7.24 (2H, m), 7.19 (2H, d, J = 9 Hz), 5.84 (1H, S), 2.85 (3H, s); MS m/z 401.0 [M+H]+
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CpcI Name & Data
234 N-[4-(difluoromethoxy)phenyl]-2-(2-methyl-l H-benzimidazol-1 -yl)pyrimidine-4,6diamine ’H NMR (500 MHz, Methanol-^) δ ppm 8.11 (1H, m), 7.57 (1H, m), 7.45 (2H, d, 7 Hz), 7.25 (2H, m), 7.09 (2H, d, J = 9 Hz), 5.48 (1H, S), 2.85 (3H, s); MS m/z 383.1 [M+H]+
235 N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine- 4,6-diamine ‘H NMR (500 MHz, Mcthanol-0/4) δ ppm 8.10 (1H, m), 7.58-7.54 (2H, m), 7.27-7.14 (4H, m), 5.47 (1H, s), 2.85 (3H, s); MS m/z 401.0 [M+H]+
263 N-(4-chlorophenyl)-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine NMR (500 MHz, Acetone-^) δ ppm 8.59 (s, 1H), 8.05 (dd, J = 2.52, 10.40 Hz, 1H), 7.47 - 7.61 (m, 4H), 7.31 - 7.42 (m, 2H), 6.92 - 7.08 (m, 1H), 6.37 (br. s., 1H), 5.93 (s, 1H), 2.77 - 2.88 (m, 3H); m.p.: 183-185; MS m/z 369.0 [M+H]+
264 2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine ‘H NMR (500 MHz, Acetonc-R) δ ppm 8.37 (br. s., 1H), 8.10 (dd, J= 2.52,10.40 Hz, 1H), 7.52 (dd, J= 5.04, 8.83 Hz, 1H), 7.34 (d, J= 8.20 Hz, 2H), 7.18 (d, J= 8.20 Hz, 2H), 6.94 - 7.07 (m, 1H), 6.27 (br. s„ 2H), 5.82 - 5.96 (m, 1H), 2.85 (s, 3H), 2.32 (s, 3H); m.p.: 210-212; MS m/z 349.0 [M+H]+
266 N-[4-(dimethylamino)phenyl]-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine4,6-diamine 'll NMR (500 MHz, Acetone-i76) δ ppm 8.11 - 8.16 (m, 1H), 8.07 - 8.10 (m, 1H), 7.47 7.56 (m, 1H), 7.23 (d, /= 9.77 Hz, 2H), 6.94 - 7.05 (m, 1H), 6.79 (d, J= 8.83 Hz, 2H), 6.09 - 6.25 (br, s, 2H), 5.67 (s, 1H), 2.94 (s, 6H), 2.85 (s, 3H); m.p.: 122-125; MS m/z 378.0 [M+H]+
267 N-(4-chloro-3 -fluorophenyl)-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6diamine fH NMR (500 MHz, Acetone-/^) δ ppm 8.80 (s, 1H), 8.03 (dd, J-2.52, 10.09 Hz, 1H), 7.67 (dd, J= 2.36, 11.82 Hz, 1H), 7.54 (dd, J= 5.04, 8.51 Hz, 1H), 7.44 (t, /= 8.67 Hz, 1H), 7.27 - 7.37 (m, 1H), 6.95 - 7.09 (m, 1H), 6.46 (br. s., 2H), 5.99 (s, 1H), 2.85 (s, 3H); m.p.: 225-227; MS m/z 387.0 [M+H]+
268 2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(3-methylphenyl)pyrimidine-4,6-diamine Ή NMR (500 MHz, Acetone-/^) δ ppm 8.37 - 8.52 (m, 1H), 8.14 (dd, J= 2.68, 10.25 Hz, 1H), 7.55 (dd, J= 5.20, 8.67 Hz, 1H), 7.40 (br. s., 1H), 7.22 - 7.30 (m, 2H), 7.00 - 7.11 (m, 1H), 6.94 (d, J= 6.62 Hz, 1H), 6.27 - 6.40 (s, 2H), 5.91 - 6.06 (s, 1H), 2.89 (s, 3H), 2.34 (s, 3H); m.p.: 203-205; MS m/z 349.0 [M+H]+
269 N-(2,2-difluoro-l,3-benzodioxol-5-yl)-2-(6-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-/^) δ ppm 8.62 (s, 1H), 8.04 (dd, J = 2.52, 10.40 Hz, 1H), 7.56 (d, /= 1.89 Hz, 1H), 7.53 (dd, J= 5.04, 8.83 Hz, 1H), 7.21 - 7.29 (m, 2H), 6.97 - 7.05 (m, 1H), 6.38 (br. s., 2H), 5.91 (s, 1H), 2.83 (s, 3H); m.p.: 212-215; MS m/z 415.0 [M+H]+
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Example 9
2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine (Cpd 154)
Figure AU2013348009C1_D0170
Figure AU2013348009C1_D0171
A mixture of 2-methyl-3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)pyrazolo[l,5a]pyridine (53 mg, 0.205 mmol), di-tert-butyl 2-chloro-6-(4(trifluoromethyl)phenylamino)pyrimidin-4-yliminodicarbonate (110 mg, 0.225 mmol), tris(dibenzylideneacetone) dipalladium(O) (18 mg, 0.02 mmol) tricyclohexylphosphine (14 mg, 0.051 mmol), and potassium phosphate (87.0 mg, 0.41 mmol) in dioxane (3.5 mL) and water (0.1 mL) was degassed by purging with argon, and then was heated at 85°C for 3 hours. The solution was cooled and filtered via plug of Celite. The filtrate was concentrated and purified by silica gel column chromatography giving tert-butyl 3,3-dimethylbutanoyl(2-(2methylpyrazolo[l,5-a]pyridin-3-yl)-6-(4-(trifluoromethyl)phenylamino)-pyrimidin-4yl)carbamate (25mg, 21%) as a clear oil, which was dissolved in dichloromethane (1 mL) and treated with TFA (0.1 mL) at 0°C. The resulting mixture was stirred at room temperature for 4 hours. The solvent was concentrated, and the residual material was partitioned between ethyl acetate and a saturated NaHCO3 solution. The organic layer was separated, dried over Na2SO4, then filtered and evaporated. The residual material was triturated with ethyl ether to afford the title compound as a yellow solid (8 mg, 50%).
!H NMR (500 MHz, Acetone-^) δ ppm 8.55 (d, J = 8.8 Hz, 1H), 8.42 (br. s., 1H), 8.37 (d, J = 6.6 Hz, 1H), 7.70 (d, J = 8.8 Hz, 2H), 7.50 (d, J = 8.5 Hz, 2H), 7.13 (ddd, J = 8.4, 7.3, 0.8 Hz, 1H), 6.77 (td, J = 6.6, 1.6 Hz, 1H), 5.82 (br. s., 2H), 5.77 (s, 1H), 2.66 (s, 3H); MS m/z 385.3 [M+H]+.
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Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 9 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
70 N-[4-(trifluoromethyl)phenyl]-2-(1,3,5-trimethyl-lH-pyrazol-4-yl)pyrimidine-4,6-diamine ‘H NMR (500 MHz, CDC13) δ ppm 7.54 (2H, d, J = 8.7 Hz), 7.48 (2H, d, J = 8.7 Hz), 5.86 (1H, s), 5.60 (2H, v br), 3.73 (3H, s), 2.53 (3H, s), 2.50 (3H, s); m.p. 270-271 °C; MS m/z 363.0 [M+H]+
Example 10
5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6diamine (Cpd 179)
F j NH ^S^NH2
MeO2C^CO2Me
NaOMe
MeOH
OH
Figure AU2013348009C1_D0172
POCI3
PCI5 (cat.)
Figure AU2013348009C1_D0173
aq. MeOH
MPS
Figure AU2013348009C1_D0174
Step 1. To a solution of methyl carbamimidothioate-(H2SO4)i/2 salt (45.90 g, 0.33 mol) and dimethyl 2-fluoromalonate (45.03 g, 0.30 mol) in MeOH (450 mL) at 0°C was slowly added sodium methoxide (4.37 M in MeOH, 226 mL, 0.99 mol). The mixture was stirred for 16 hours at room temperature. The solution was concentrated under reduced pressure. The resulting slurry was diluted with water (50 mL) and acidified to about pH 2 by using a 6N HC1 solution. The resulting precipitate was collected, washed with water and dried under vacuum to give 5-fhioro-2-(methylthio)pyrimidine-4,6-diol (46.85 g, 88%).
To a solution of 5-fluoro-2-(methylthio)pyrimidine-4,6-diol (13.2 g, 74.9 mmol) in POCI3 (60 mL) was added a catalytic amount of PCI5 (60 mg). The mixture was heated at 100°C for 16 hours and then concentrated under reduced pressure. To the mixture was carefully added ice water (150 mL). The resulting precipitate was removed by filtration, washed with water, then dried under nitrogen to give 4,6-dichloro-5-fluoro-2(methylthio)pyrimidine (13.5 g, 85%).
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To a solution of 4,6-dichloro-5-fluoro-2-(methylthio)pyrimidine (12.4 g, 58.8 mmol) in MeOH (150 mL) was added potassium peroxymonosulfate ^KHSOs-KHSCfi-KzSCfi) (108.7 g, 176.4 mmol) and water (70 mL). The mixture was stirred for 6 hours at room temperature. The salt was removed by filtration, then washed with MeOH until no more 5 product was observed. The combined organic mixture was concentrated then ice water was added to the mixture to provide a precipitate, which was filtered and washed by water. The solid was dried under nitrogen to yield 4,6-dichloro-5-fluoro-2-(methylsulfonyl)pyrimidine as a white solid (14.6 g, 99%).
Cl
Figure AU2013348009C1_D0175
20% DMF/THF
Step 2. A solution of 4-fluorobenzene-l,2-diamine (3.78 g, 30 mmol) in acetic acid (10.0 mL) was microwaved for 1 hour at 180°C. The mixture was concentrated under reduced pressure and triturated with ether to yield 6-fluoro-2-methyl-lH-benzo[d]imidazole as a brownish solid (4.31 g, 88%).
To a solution of 6-fluoro-2-methyl-lH-benzo[d]imidazole (2.31 g, 15.4 mmol) in
THF (50 mL) and DMF (10 mL) at -78°C was added 60% NaH (648 mg, 16.2 mmol). The mixture was stirred for about 10 minutes at room temperature. To the mixture at -78°C was added 4,6-dichloro-5-fluoro-2-(methylsulfonyl)pyrimidine (3.74 g, 15.3 mmol) in one portion, then the mixture was stirred at -78°C for 15 minutes. The reaction mixture was quenched with a IM HC1 solution (18 mL) and a crude mixture was extracted with EtOAc (200 mL). The organic layer was concentrated under reduced pressure, and purified by column chromatography (5-30% EtOAc/hexanes) to give l-(4,6-dichloro-5-fluoropyrimidin2-yl)-6-fluoro-2-methyl-lH-benzo[d]imidazole as a white solid (1.83 g, 38%).
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Figure AU2013348009C1_D0176
Step 3. The mixture of 1 -(4,6-dichloro-5-fluoropyrimidin-2-yl)-6-fluoro-2-methyllH-benzo[d]-imidazole (63 mg, 0.2 mmol) and 4-methoxyaniline (49 mg, 0.4 mmol) in EtOH (1 mL) was stirred for 1 hour at 60°C. The precipitate was obtained by adding water (10 mL). The product (6-chloro-5-fluoro-2-(6-fluoro-2-methyl-1 H-benzo[d]imidazol-1 -yl)-N-(4methoxyphenyl)-pyrimidin-4-amine) was removed by filtration and washed with water several times. The resulting crude 6-chloro-5-fluoro-2-(6-fluoro-2-methyl-lHbenzo[d]imidazol-l-yl)-N-(4-methoxyphenyl)pyrimidin-4-amine was used in the next step without further purification.
To the crude product in DMSO (5 mL) was added 14 M aqueous NH4OH (3 mL). The suspended mixture was heated for 18 hours at 100°C until all the starting material was consumed. After cooling to room temperature, water (10 mL) was added to the mixture to form a precipitate. The precipitate was isolated by filtration and washed with water several times. The resulting product was dried under nitrogen to give the title compound as an offwhite solid (72 mg, 94%).
‘id NMR (500 MHz, Acetone-^) δ ppm 8.30 (1H, br. s.) 7.94 (1H, dd, 7=9.93, 2.36 Hz) 7.48 - 7.56 (3H, m) 6.93 - 7.05 (3H, m) 6.48 (2H, br. s.) 3.83 (3H, s) 2.75 (3H, s); MS m/z 383.2 [M+H]+.
Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 10 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
95 5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine 'H NMR (500 MHz, DMSO-76) δ ppm 9.60 (1H, s) 8.02 (1H, dd, 7=7.25, 2.21 Hz) 7.86 (2H, d, 7=8.51 Hz) 7.65 (2H, d, 7=8.51 Hz) 7.56 - 7.60 (1H, m) 7.29 (2 H, s) 7.17 - 7.26 (2H, m) 2.75 (3H, s); MS m/z 403.2 [M+H]+
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106 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine4,6-diamine ’H NMR (500 MHz, Acetone-^) δ ppm 8.39 (1H, s) 7.97 (1H, d, 7=7.88 Hz) 7.59 - 7.64 (2H, m) 7.42 (1H, d, 7=7.25 Hz) 7.01 - 7.11 (4H, m) 6.83 (1H, t, 7=74.56 Hz) 6.40 (2H, br. s.) 2.63 (3H, s); MS m/z 401.1 [M+H]+
107 2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6- diamine *H NMR (500 MHz, Acetone-^) δ ppm 8.69 (1H, br. s.) 7.91 (1H, d, 7=7.88 Hz) 7.85 (2H, d, 7=8.51 Hz) 7.53 (2H, d, 7=8.51 Hz) 7.47 (1H, d, 7=6.94 Hz) 7.02 - 7.13 (2H, m) 6.54 (2H, br. s.) 3.14 (2H, q, 7=7.36 Hz) 1.20 (3H, t); MS m/z 417.1 [M+H]+
108 5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 'Η NMR (500 MHz, Acetone-7rt) δ ppm 8.85 (1H, br. s.) 8.13 (1H, dd, 7=9.46, 5.04 Hz) 7.98 (2H, d, 7=8.51 Hz) 7.71 (2H, d, 7=8.51 Hz) 7.31 (1H, dd, 7=9.62, 2.36 Hz) 6.96 7.04 (1H, m) 6.72 (2H, br. s.) 2.82 (3H, s); MS m/z 421.1 [M+H]+
109 5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamme ‘11 NMR (500 MHz, Acetone-70) δ ppm 8.85 (1H, br. s.) 7.89 - 8.00 (3H, m) 7.71 (2H, d, 7=8.51 Hz) 7.56 (1H, dd, 7=8.83, 5.04 Hz) 7.02 - 7.08 (1H, m) 6.76 (2H, br. s.) 2.82 (3H, s); MS m/z 421.1 [M+H]+
110 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-76) δ ppm 8.01 (1H, dd, 7=10.40, 2.21 Hz) 7.81 (1H, br. s.) 7.68 - 7.72 (2H, m) 7.65 (1H, dd, 7=8.83, 5.04 Hz) 7.26 - 7.31 (2H, m) 7.12 - 7.18 (1H, m) 6.87 (1H, t, 7=74.56 Hz) 5.87 (2H, br. s.) 2.87 (3H, s); MS m/z 419.1 [M+H]+
111 N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol1 -yl)pyrimidine-4,6-diamine *H NMR (500 MHz, Acetonc-76) δ ppm 8.73 (1H, s) 7.93 (1H, dd, 7=9.93, 2.36 Hz) 7.80 (1H, dd, 7=12.93, 2.52 Hz) 7.51 - 7.59 (2H, m) 7.36 (1 H, t, 7=8.99 Hz) 7.01 - 7.08 (1H, m) 6.98 (1H, t, 7=73.77 Hz) 6.71 (2H, br. s.) 2.81 (3H, s); MS m/z 437.1 [M+H]+
112 N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(5-fluoro-2-methyl-l H-benzimidazol1 -yl)pyrimidine-4,6-diamine 'H NMR (500 MHz, Acetonc-i#) δ ppm 8.19 (1H, dd, 7=9.46, 5.04 Hz) 7.94 (1H, br. s.) 7.79 (1H, dd, 7=12.93, 2.52 Hz) 7.35 - 7.50 (3H, m) 7.09 - 7.16 (1H, m) 6.87 (1H, t, Hz) 5.91 (2H, s) 2.90 (3H, s); MS m/z 437.2 [M+H]+
113 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-#^ δ ppm 8.19 (1H, dd, 7=9.46, 5.04 Hz) 7.81 (1H, br. s.) 7.67.7.74 (2H, m) 7.42 (1H, dd, 7=9.46, 2.84 Hz) 7.25 - 7.32 (2H, m) 7.07 - 7.16 (1H, m) 6.88 (1H, t, 7=74.56 Hz) 5.84 (2H, s) 2.88 (3H, s); MS m/z 419.1 [M+H]+
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Cpd Name & Data
114 2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-^) δ ppm 8.91 (1H, s) 8.57 - 8.58 (1H, m) 8.39 (1H, d, 7=2.21 Hz) 7.93 (2H, d, 7=8.51 Hz) 7.75 (2H, d, 7=8.51 Hz) 6.83 (2H, br. s.) 2.93 (3H, s); MS m/z 438.3 [M+H]+
115 2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidme-4,6-diamine JH NMR (500 MHz, Acetone-76) δ ppm 8.47 (1H, br. s.) 8.41 (1H, d, 7=2.21 Hz) 8.23 (1H, d, 7=2.52 Hz) 7.55 (2H, d, 7=8.83 Hz) 7.11 (2H, d, 7=9.14 Hz) 6.85 (1H, t, 7=74.10 Hz) 6.55 (2H, br. s.) 2.74 (3H, s); MS m/z 436.2 [M+H]+
116 2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]-5-fluoropyrimidine-4,6-diamme ’H NMR (500 MHz, Acetone-^) δ ppm 8.77 (1H, s) 8.56 (1H, d, 7=2.21 Hz) 7.73 (1H, dd, 7=12.61, 2.52 Hz) 7.50 - 7.56 (1H, m) 7.39 (1H, t, 7=8.99 Hz) 7.00 (1H, t, 7=73.61 Hz) 6.79 (2H, br. s.) 2.91 (3H, s); MS m/z 454.1 [M+H]+
117 2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-^) δ ppm 8.90 (1H, s) 8.22 - 8.34 (2 H, m) 7.99 (2H, d, 7=8.20 Hz) 7.71 (2H, d, 7=8.20 Hz) 6.84 (2H, br. s.) 3.20 - 3.29 (1H, m) 1.26 - 1.34 (2H, m) 1.06 - 1.12 (2H, m); MS m/z 448.1 [M+H]+
119 N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine 'H NMR (500 MHz, Acetone-76) δ ppm 8.71 (1H, br. s.) 8.12 (1H, d, 7=8.51 Hz) 7.87 (1H, dd, 7=13.08, 2.68 Hz) 7.52 - 7.62 (2H, m) 7.34 (1H, t, 7=8.99 Hz) 7.17 - 7.27 (2H, m) 6.98 (1H, t, 7=73.93 Hz) 6.65 (2H, br. s.) 2.81 (3H, s); MS m/z 419.3 [M+H]+
120 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidme-4,6-diamine Ή NMR (500 MHz, Acetone-7,) δ ppm 8.85 (1H, br. s.) 8.06 (2H, d, 7=8.51 Hz) 8.00 (1H, dd, 7=7.25, 1.26 Hz) 7.67 (2H, d, 7=8.51 Hz) 7.50 - 7.56 (1H, m) 7.14 - 7.25 (2H, m) 6.70 (2H, br. s.) 2.96 - 3.05 (1H, m) 1.20 - 1.26 (2H, m) 1.00 - 1.06 (2H, m); MS m/z 429.2 [M+H]+
121 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine JH NMR (500 MHz, Acetone-76) δ ppm 8.40 (1H, s) 7.86 (1H, dd, 7=7.72, 1.73 Hz) 7.63 - 7.70 (2H, m) 7.36 (1H, d, 7=9.14 Hz) 6.98 - 7.08 (4H, m) 6.64 - 6.97 (1H, m) 6.41 (2H, s) 2.83 - 2.91 (1H, m) 1.01 - 1.07 (2H, m) 0.80 - 0.87 (2H, m); MS m/z 427.2 [M+H]+
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Cpd Name & Data
122 2-(2-cyclopropyl-l H-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3-fluorophenyl]-5fluoropyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-;^) δ ppm 8.73 (1H, s) 7.96 - 8.03 (2H, m) 7.50 - 7.60 (2H, m) 7.32 (1H, t, >8.83 Hz) 7.20 (2H, dtd, >19.70, 7.33, 7.33, 1.26 Hz) 6.80 - 7.13 (2H, m) 6.66 (2H, s) 2.97 - 3.05 (1H, m) 1.23 (2H, dd, >5.04, 2.84 Hz) 1.01 - 1.08 (2H, m); MS m/z 445.2 [M+H]+
123 N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine4,6-diamine *H NMR (500 MHz, Acetone-^) δ ppm 8.52 - 8.56 (1H, s) 8.04 - 8.09 (1H, m) 7.76 (2H, d, >9.14 Hz) 7.57 - 7.61 (1H, m) 7.19 (4H, d, >8.83 Hz) 6.97 (1H, m) 6.49 - 6.58 (2H, s) 3.25 (2H, d, >7.57 Hz) 1.29 - 1.34 (3H, m); MS m/z 415.3 [M+H]+
124 N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine !H NMR (500 MHz, Acctone-JQ δ ppm 8.72 (1H, s) 8.05 - 8.09 (1H, m) 7.87 (1H, dd, >12.93, 2.52 Hz) 7.59 - 7.63 (1H, m) 7.54 (1H, ddd, >8.91, 2.60, 1.42 Hz) 7.33 (1H, t, >8.83 Hz) 7.18 - 7.27 (2H, m) 6.98 (1H, t, >74.70 Hz) 6.64 (2H, s) 3.28 (2H, q, >7.36 Hz) 1.35 (3H, t, >7.90 Hz); MS m/z 433.3 [M+H]+
125 2-(5,6-difluoro-2-methyl-1 H-benzimidazol-1-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 'll NMR (500 MHz, Acetone-^) δ ppm 8.69 - 8.75 (1H, m) 7.97 - 8.04 (1H, m) 7.76 7.83 (2H, m) 7.55 - 7.61 (2H, m) 7.30 - 7.37 (1H, m) 6.59 - 6.69 (2H, m) 2.68 (3H, s); MS m/z 439.2 [M+H]+
126 N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-lyl)-5-fluorppyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-^) δ ppm 8.72 - 8.76 (1H, m) 8.12 - 8.18 (1H, m) 7.74 7.80 (1H, m) 7.45 - 7.55 (2H, m) 7.34 - 7.40 (1H, m) 6.90 - 7.05 (1H, m) 6.69 - 6.78 (2H, m) 2.82 (3H, s); MS m/z 455.2 [M+H]+
127 2-(4,6-difluoro-2-methyl-lH-benzimidazol-1 -yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-^) δ ppm 8.85 - 8.90 (1H, m) 7.93 - 7.99 (2H, m) 7.77 7.82 (1H, m) 7.72 (2H, s) 6.90 - 6.97 (1H, m) 6.73 - 6.84 (2H, m) 2.83 (3H, s); MS m/z 439.2 [M+H]+
128 N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-lyl)-5-fluoropyrimidine-4,6-diamine rH NMR (500 MHz, Acetone» 8 ppm 8.71 - 8.79 (1H, m) 7.74 - 7.82 (2H, m) 7.48 - 7.55 (1H, m) 7.33 - 7.40 (1H, m) 6.83 - 7.15 (3H, m) 6.70 - 6.79 (2H, m) 2.82 (3H, s); MS m/z 455.2 [M+H]+
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Cpd Name & Data
129 2-(2-ethyl-4,6-difluoro-1 H-benzimidazol-1 -yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-70) 5 ppm 8.89 (1H, s) 7.95 (2H, d, 7=8.51 Hz) 7.66 - 7.77 (3H, m) 6.90 - 6.98 (1H, m) 6.79 (2H, br. s.) 3.30 (2H, q, 7=7.57 Hz) 1.34 (3H, t, 7=7.41 Hz); MS m/z 453.2 [M+H]+
130 N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)5-fluoropyrimidine-4,6-diamine 'bl NMR (500 MHz, Acetonc-76) δ ppm 8.75 (1H, s) 7.72 - 7.81 (2H, m) 7.51 (1H, ddd, 7=8.91, 2.60, 1.42 Hz) 7.35 (1H, t, 7=8.83 Hz) 6.81 - 7.14 (2H, m) 6.74 (2H, br. s.) 3.28 (2H, q, 7=7.25 Hz) 1.34 (3H, t, 7=7.41 Hz); MS m/z 469.2 [M+H]+
131 N-[4-(difluoromethoxy)phenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine 'bl NMR (500 MHz, Acetone-/,) δ ppm 8.59 (1H, s) 7.79 (1H, ddd, 7=9.85, 2.44, 0.95 Hz) 7.69 - 7.74 (2H, m) 7.20 - 7.24 (2H, m) 6.81 - 7.13 (2H, m) 6.65 (2H, br. s.) 2.78 (3H, s); MS m/z 437.2 [M+H]1
132 N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine ’ll NMR (500 MHz, Acetone-/;) δ ppm 8.59 (1H, s) 7.75 (1H, ddd, 7=9.77, 2.21, 0.95 Hz) 7.68 - 7.72 (2H, m) 7.18 - 7.25 (2H, m) 6.81 - 7.13 (2H, m) 6.65 (2 H, s) 3.25 (2H, q, 7=7.57 Hz) 1.28 - 1.33 (3H, m); MS m/z 451.2 [M+H]+
133 N-[4-(difluoromethoxy)phenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine JH NMR (500 MHz, Acetone-/) δ ppm 8.57 (1H, br. s.) 8.15 (1H, dd, 7=11.82, 7.72 Hz) 7.68 - 7.74 (2H, m) 7.46 (1H, dd, 7=10.72, 7.57 Hz) 7.21 - 7.26 (2H, m) 7.05 (2H, t, 7=76.30 Hz) 6.65 (2H, s) 2.78 (3H, s); MS m/z 437.3 [M+H]+
134 5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine JH NMR (500 MHz, Acetone-/) δ ppm 8.87 (1H, br. s.) 7.99 (2H, d, 7=8.51 Hz) 7.92 (1H, d, 7=8.20 Hz) 7.69 (2H, d, 7=8.51 Hz) 7.19 (1H, td, 7=8.20, 5.04 Hz) 7.01 (1H, dd, 7=10.72, 7.25 Hz) 6.74 (2H, br. s.) 2.83 (3H, s); MS m/z 421.2 [M+H]+
135 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol-l- yl)pyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-/) δ ppm 8.57 (1H, s) 7.92 (1H, d, 7=9.14 Hz) 7.72 - 7.78 (2H, m) 6.80 - 7.24 (5H, m) 6.59 (2H, br. s.) 2.79 (3H, s); MS m/z 418.2 [M+H]+
136 N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol- 1 -yl)pyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-/) δ ppm 8.74 (1H, s) 7.93 (1H, d, 7=7.57 Hz) 7.85 (1H, dd, 7=12.93, 2.52 Hz) 7.51 - 7.57 (1H, m) 7.34 (1H, t, 7=8.99 Hz) 6.82 - 7.23 (3H, m) 6.69 (2H, s) 2.86 (3H, s); MS m/z 437.2 [M+H]+
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Cpd Name & Data
137 5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-76) δ ppm 8.88 (1H, br. s.) 8.47 (1H, dd, 7=8.04, 1.73 Hz) 8.40 - 8.44 (1H, m) 7.92 - 8.00 (2H, m) 7.72 (2H, d, 7=8.51 Hz) 7.18 - 7.23 (1H, m) 6.70 - 6.80 (2H, m) 2.90 (3H, s); MS m/z 404.2 [M+H]+
138 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridin-lyl)pyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-76) δ ppm 8.58 (1H, s) 8.46 (1H, dd, 7=8.20, 1.58 Hz) 8.40 (1H, dd, 7=4.73, 1.58 Hz) 7.70 - 7.76 (2H, m) 7.21 - 7.25 (2H, m) 7.15 - 7.19 (1H, m) 6.99 (2H, s) 6.56 - 6.66 (2H, m) 2.86 (3H, s); MS m/z 402.2 [M+H]+
139 N-[4-(difluoromethoxy)-3-fluorophenyl]-5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridinl-yl)pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-76) δ ppm 8.75 (1H, br. s.) 8.45 - 8.50 (1H, m) 8.42 (1H, dd, 7=4.73, 1.58 Hz) 7.80 (1H, dd, 7=12.61, 2.52 Hz) 7.53 (1H, dt, 7=9.06, 1.93 Hz) 7.37 (1H, t, 7=8.83 Hz) 7.20 (1H, dd, 7=8.20, 4.73 Hz) 6.83 - 7.16 (2H, m) 6.72 (2H, br. s.) 2.89 (3H, s); MS m/z 420.2 [M+H]+
140 2-(2-cyclopropyl-4-fluoro-l H-benzimidazol-1 -yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine '14 NMR (500 MHz, Acetone-76) δ ppm 8.88 (1H, s) 8.05 (2H, d, 7=8.51 Hz) 7.81 (1H, dd, 7=8.20, 0.63 Hz) 7.67 (2H, d, 7=8.51 Hz) 7.16 (1H, td, 7=8.12, 4.89 Hz) 6.95 - 7.02 (1H, m) 6.74 (2H, s) 2.96 - 3.03 (1H, m) 1.24 - 1.29 (2H, m) 1.03 - 1.08 (2H, m); MS m/z 447.2 [M+H]+
141 2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-7rt) δ ppm 8.59 (1H, s) 7.77 - 7.84 (3H, m) 7.16 - 7.20 (2H, m) 7.12 - 7.16 (1H, m) 6.81 - 7.11 (2H, m) 6.61 (2H, s) 3.01 (1H, tt, 7=8.28, 4.97 Hz) 1.20 - 1.24 (2H, m) 1.03 (2H, dq, 7=8.32, 3.43 Hz); MS m/z 445.2 [M+H]+
142 2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]-5-fluoropyrimidine-4,6-diamine 'Η NMR (500 MHz, Acetone-76) δ ppm 8.77 (1H, s) 7.99 (1H, dd, 7=12.93, 2.52 Hz) 7.83 (1H, dd, 7=8.20, 0.95 Hz) 7.57 (1H, ddd, 7=9.06, 2.60, 1.58 Hz) 7.33 (1H, t, 7=8.99 Hz) 7.18 (1H, td, 7=8.12, 4.89 Hz) 6.83 - 7.13 (2H, m) 6.72 (2 H, s) 3.01 (1H, tt, 7=8.28, 4.97 Hz) 1.23 - 1.30 (2H, m) 1.08 (2H, dq, 7=8.32, 3.43 Hz); MS m/z 463.2 [M+H]+
155 2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(difluoromethoxy)phenyl]-5-fluoropyrimidine-4,6-diamine 'H NMR (500 MHz, Acetone-76) δ ppm 8.62 (1H, s) 8.23 - 8.32 (2H, m) 7.72 - 7.78 (2H, m) 7.18 - 7.24 (2H, m) 6.98 (1H, t, 7=75.30 Hz) 6.71 (2H, br. s.) 3.27 (1H, tt, 7=8.28, 4.97 Hz) 1.25 (2H, dd, 7=4.89, 3.00 Hz) 1.05 (2H, dd, 7=8.20, 3.15 Hz); MS m/z 446.2 [M+H]+
150
WO 2014/081906
PCT/US2013/071132
Cpd Name & Data
158 2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-76) δ ppm 8.82 (1H, d, 7=1.58 Hz) 8.11 (1H, d, 7=8.20 Hz) 7.92 - 7.99 (2H, m) 7.69 (2H, d, 7=8.51 Hz) 7.58 (1H, d, 7=2.21 Hz) 7.19 (1H, dd, 7=8.83, 2.21 Hz) 6.70 (2H, br. s.) 2.82 (3H, s); MS m/z 437.2 [M+H]+
159 2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine '11 NMR (500 MHz, Acetone-^) δ ppm 8.42 (1H, s) 7.95 - 8.00 (1H, m) 7.55 - 7.62 (2H, m) 7.43 (1H, d, 7=1.58 Hz) 7.01 - 7.10 (3H, m) 6.84 (1H, t, 7=75.30 Hz) 6.44 (2H, br. s.) 2.64 (3H, s); MS m/z 435.2 [M+H]+
160 2-(6-chloro-2-methyl-lH-benzirnidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-76) δ ppm 8.83 (1H, br. s.) 8.19 (1H, d, 7=1.58 Hz) 7.94 (2H, d, 7=8.20 Hz) 7.70 (3H, d, 7=8.51 Hz) 7.55 (1H, d, 7=8.51 Hz) 7.21 - 7.27 (1H, m) 6.72 (2H, br. s.) 2.82 (3H, s); MS m/z 437.2 [M+H]+
161 2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine ’ll NMR (500 MHz, Acetone-70 δ ppm 8.57 (1H, s) 8.17 - 8.22 (1H, m) 7.70 - 7.77 (2H, m) 7.55 (1H, d, 7=8.20 Hz) 7.20 - 7.26 (3H, m) 6.97 (1H, t, 7=74.70 Hz) 6.62 (2H, br. s.) 2.80 (3H, s); MS m/z 435.2 [M+H]+
162 2-(2-ethyl-5-fluoro-l H-benzimidazol-1-yl)-5-fluoro-N-[4(trifluOromethyl)phenyl]pyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone^) δ ppm 8.85 (1H, br. s.) 8.08 (1H, dd, 7=8.67, 5.20 Hz) 7.97 (2H, d, 7=8.20 Hz) 7.64 - 7.73 (2H, m) 7.33 (1H, d, 7=6.62 Hz) 6.98 - 7.04 (1H, m) 6.72 (2H, br. s.) 3.29 (2H, q, 7=7.36 Hz) 1.34 (3H, t, 7=8.20 Hz); MS m/z 435.3 [M+H]+
163 N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-5-fluoro-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-^) δ ppm 8.56 (1H, s) 8.09 (1H, dd, 7=9.46, 5.04 Hz) 7.69 - 7.75 (2H, m) 7.31 (1H, dd, 7=9.30, 2.68 Hz) 7.18 - 7.24 (2H, m) 6.81 - 7.14 (2H, m) 6.57 (2H, br. s.) 3.22 - 3.29 (2H, m) 1.27 - 1.34 (3H, m); MS m/z 433.3 [M+H]+
164 2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-Tj δ ppm 8.85 (1H, s) 7.96 (2H, d, 7=8.51 Hz) 7.89 (1H, dd, 7=10.09, 2.52 Hz) 7.70 (2H, d, 7=8.51 Hz) 7.59 (1H, dd, 7=8.51, 5.04 Hz) 7.01 - 7.09 (1H, m) 6.75 (2H, br. s.) 3.29 (2H, q, 7=7.46 Hz) 1.33 (3H, t, 7=14.80 Hz); MS m/z 435.3 [M+H]+
165 N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine 'H NMR (500 MHz, Acetone-76) δ ppm 8.56 (1H, s) 7.90 (1H, dd, 7=10.40, 2.52 Hz) 7.68 - 7.75 (2H, m) 7.56 (1H, dd, 7=8.83, 5.04 Hz) 7.18 - 7.26 (2H, m) 6.81 - 7.12 (2H, m) 6.61 (2H, br. s.) 3.25 (2H, q, 7=7.46 Hz) 1.26 - 1.34 (3H, m); MS m/z 433.3 [M+H]+
151
WO 2014/081906
PCT/US2013/07U32
Cpd Name & Data
172 5 -methyl-2-(2-methyl-1 H-benzimidazol- l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine !H NMR (500 MHz, Acetone-d6) δ ppm 8.19 (1H, s) 8.14 (1H, dt, 7=8.20, 0.95 Hz) 7.87 (2H, d, 7=8.51 Hz) 7.64 (2H, d, 7=8.51 Hz) 7.55 - 7.60 (1H, m) 7.22 (1H, ddd, 7=8.04, 7.09, 1.26 Hz) 7.15 (1H, ddd, 7=8.28, 7.17, 1.26 Hz) 6.31 (2H, br. s.) 2.80 (3H, s) 2.22 (3H, s); MS m/z 399.2 [M+H]+
183 5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[6-(trifluoromethyl)pyridin-3yl]pyrimidine-4,6-diamine Ή NMR (Methanol-d4) δ ppm 8.92 (1H, d, J = 2.5 Hz), 8.34 (1H, dd, J = 8.5, 2.4 Hz), 7.81 (1H, dd, J = 9.8, 2.5 Hz), 7.75 (1H, d, J = 8.7 Hz), 7.54 (1H, dd, J = 8.7, 5 Hz), 7.06 (1H, td, J = 9.2, 2.5 Hz), 2.82 (3H, s); MS m/z 422.3 [M+H]+
184 5-fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)-N-(4-methylphenyl)pyrimidine-4,6diamine 'Η NMR (500 MHz, Acetone-^) δ ppm 8.37 (br. s., 1H), 7.94 (dd, J = 10.4, 2.5 Hz, 1H), 7.50 - 7.58 (m, 3H), 7.20 (d, J = 8.2 Hz, 2H), 7.01 (ddd, J = 9.8, 8.8, 2.5 Hz, 1H), 6.52 (br. s., 2H), 2.78 (s, 3H), 2.34 (s, 3H); MS m/z 367.2 [M+H]+
185 N-(4-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6diamine 1H NMR (500 MHz, Acetone-d^) δ ppm 8.58 (br. s., 7H), 7.93 (dd, J = 10.2, 2.7 Hz, 1H), 7.70 - 7.76 (m, 2H), 7.54 (dd, J = 8.7, 5.2 Hz, 1H), 7.37 - 7.42 (m, 2H), 7.03 (ddd, J = 9.8, 8.8, 2.5 Hz, 1H), 6.63 (br. s., 2H), 2.79 (s, 3H); MS m/z 387.2 [M+H]+
189 5-fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)-N-(3-methoxyphenyl)pyrimidine4,6-diamine ΓΗ NMR (500 MHz, Acetone-d^) δ ppm 8.43 (br. s., 1H), 7.97 (dd, J = 10.1, 2.5 Hz, 1H), 7.54 (dd, J = 8.8, 5.0 Hz, 1H), 7.32 - 7.37 (m, 1H), 7.23 - 7.31 (m, 2H), 7.03 (ddd, J = 9.5, 8.7, 2.8 Hz, 1H), 6.68 - 6.75 (m, 1H), 6.57 (br. s., 2H), 3.77 (s, 3H), 2.81 (s, 3H); MS m/z 383.2 [Mill]'
190 N-(3-chlorophenyl)-5-fhioro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine '11 NMR (500 MHz, Acetone-dQ δ ppm 8.63 (br. s., 1H), 7.96 (dd, J = 10.1, 2.5 Hz, 1H), 7.91 (t, J = 2.0 Hz, 1H), 7.62 (ddd, J = 8.3, 2.0, 0.8 Hz, 1H), 7.55 (dd, J = 8.8, 5.0 Hz, 1H), 7.38 (t, J = 8.0 Hz, 1H), 7.14 (ddd, J = 8.2, 2.2, 0.9 Hz, 1H), 7.04 (ddd, J = 9.5, 8.5, 2.5 Hz, 1H), 6.68 (br. s., 2H), 2.82 (s, 3H); MS m/z 387.2 [M+H]+
191 5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-d^) δ ppm 9.21 (br. s., 1H), 8.49 (dd, J = 10.2, 2.7 Hz, 1H), 8.32 - 8.42 (m, 2H), 8.10 (dd, J = 8.7, 5.2 Hz, 1H), 7.91 (dd, J = 9.1, 0.9 Hz, 2H), 7.59 (ddd, J = 9.5, 8.5, 2.5 Hz, 1H), 7.21 (br. s., 2H), 3.34 (s, 3H); MS m/z 437.2 [M+H]+
152
WO 2014/081906
PCT/US2013/071132
Cpd Name & Data
192 4- {[6-amino-5-fluoro-2-(6-fluoro-2-methyl-l H-benzimidazol-1 -yl)pyrimidin-4yljamino} benzonitrile Ή NMR (500 MHz, Acetone-/,}) δ ppm 8.79 (br. s., 1H), 7.80 - 7.86 (m, 2H), 7.78 (dd, J = 10.1, 2.5 Hz, 1H), 7.61 (dt, J = 8.8, 2.5 Hz, 2H), 7.42 (dd, J = 8.8, 5.0 Hz, 1H), 6.91 (ddd, J = 9.5, 8.5, 2.6 Hz, 1H), 6.65 (br. s„ 2H), 2.67 (s, 3H); MS m/z 378.2 [M+H]+
193 methyl 4-{[6-amino-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidin-4yl] amino (benzoate 'id NMR (500 MHz, Acetone-^) δ ppm 8.82 (br. s., 1H), 7.99 - 8.04 (m, 2H), 7.96 (dd, J = 10.1, 2.5 Hz, 1H), 7.85 - 7.90 (m, 2H), 7.56 (dd, J = 8.8, 5.0 Hz, 1H), 7.05 (ddd, J = 9.5, 8.5, 2.5 Hz, 1H), 6.73 (br. s„ 2H), 3.88 (s, 3H), 2.83 (s, 3H); MS m/z 411.2 [M+H]+
194 5-fluoro-2-(2-methyl-1 H-benzimidazol- l-yl)-N-(3-methylphenyl)pyrimidine-4,6-diamine 'Η NMR (500 MHz, Acetone-^) δ ppm 8.36 (1H, br. s.) 8.19 (1H, d, /=8.51 Hz) 7.64 (1H, s) 7.57 (1H, d, /=7.57 Hz) 7.46 (1H, dd, /=8.20, 2.21 Hz) 7.16 - 7.26 (3H, m) 6.94 (1H, d, /=7.57 Hz) 6.49 (2H, br. s.) 2.81 (3H, s) 2.33 (3H, s); MS m/z 439.2 [M+H]+
195 5-fluoro-N-(3-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6- diamine 'll NMR (500 MHz, Acetone-/^) δ ppm 8.42 (1H, br. s.) 8.13-8.18 (1H, m) 7.58 (1H, d, /=7.25 Hz) 7.40 (1H, t, /=2.21 Hz) 7.16 - 7.32 (4H, m) 6.67 - 6.71 (1H, m) 6.52 (2H, br. s.) 3.75 (3H, s) 2.82 (3H, s); MS m/z 365.2 [M+H]+
199 5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine 'H NMR (500 MHz, Acetone-rig) δ ppm 8.35 (1H, br. s.) 8.13 (1H, d, /=8.20 Hz) 7.54 7.61 (3H, m) 7.12 - 7.24 (4H, m) 6.45 (2H, br. s.) 2.78 (3H, s) 2.33 (3H, s); MS m/z 349.2 [M+H]'
200 5-fluoro-N-(4-methoxyphenyl)-2-(2 -methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6diamine rH NMR (500 MHz, Acetone-i^) δ ppm 8.28 (1H, br. s.) 8.12 (1H, d, /=8.20 Hz) 7.52 - 7.60 (3H, m) 7.12 - 7.24 (2H, m) 6.93 - 6.98 (2H, m) 6.41 (2H, br. s.) 3.82 (3H, s) 2.76 (3H, s); MS m/z 365.2 [M+H]+
201 N-(4-chlorophenyl)-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-O δ ppm 8.57 (1H, br. s.) 8.07 - 8.14 (1H, m) 7.73 - 7.80 (2H, m) 7.58 (1H, d, /=6.94 Hz) 7.35 - 7.42 (2H, m) 7.15 - 7.26 (2H, m) 6.56 (2H, br. s.) 2.79 (3H, s); MS m/z 369.:2 [M+H]+
202 4- {[6-amino-5-fluoro-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4- yl] amino } benzonitril e fH NMR (500 MHz, Acetone-/;) δ ppm 8.92 (1H, br. s.) 8.08 - 8.13 (1H, m) 7.97 - 8.03 (2H, m) 7.71 - 7.77 (2H, m) 7.56 - 7.62 (1H, m) 7.24 (2H, quind, /=7.33, 7.33, 7.33, 7.33, 1.58 Hz) 6.73 (2H, br. s.) 2.80 - 2.83 (3H, m); MS m/z 360.2 [M+H]+
153
WO 2014/081906
PCT/US2013/071132
Cpd Name & Data
203 N-(l,3-benzodioxol-5-yl)-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine !H NMR (500 MHz, Acetone-rig) δ ppm 8.33 (1H, br. s.) 8.15 (1H, d, 7=6.62 Hz) 7.56 (1H, d, 7=7.25 Hz) 7.28 (1H, d, 7=2.21 Hz) 7.16 - 7.25 (2H, m) 7.09 (1H, dd, 7=8.51, 2.21 Hz) 6.85 (1H, d, 7=8.51 Hz) 6.45 (2H, br. s.) 6.02 (2H, s) 2.79 (3H, s); MS m/z 379.2 [M+H]+
204 5-fluoro-2-(2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine4,6-diamine 'bl NMR (500 MHz, Acetone-rig) δ ppm 8.63 (1H, br. s.) 8.11 (1H, d, 7=7.57 Hz) 7.80 7.89 (2H, m) 7.57 (1H, d, 7=7.88 Hz) 7.31 - 7.38 (2H, m) 7.15 - 7.26 (2H, m) 6.58 (2H, br. s.) 2.79 (3H, s); MS m/z 419.1 [M+H]+
213 2-(5,6-difluoro-2 -methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine4,6-diamine !H NMR (500 MHz, Acetone-rig) δ ppm 8.40 (1H, br. s.) 8.15 (1H, dd, 7=11.98, 7.88 Hz) 7.49 - 7.55 (2H, m) 7.44 (1H, dd, 7=10.72, 7.57 Hz) 7.21 (2H, d, 7=8.20 Hz) 6.55 (2H, br. s.) 2.79 (3H, s) 2.35 (3H, s); MS m/z 385.2 [M+H]+
214 2-(5,6-difluoro-2-methyl-l H-benzimidazol-1 -yl)-5-fluoro-N-(4methoxyphenyl)pyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-rig) δ ppm 8.30 (1H, br. s.) 8.12 (1H, dd, 7=11.98, 7.88 Hz) 7.46 - 7.51 (2H, m) 7.41 (1H, dd, 7=10.72, 7.57 Hz) 6.93 - 6.98 (2H, m) 6.48 (2H, br. s.) 3.81 (3H, s) 2.75 (3H, s); MS m/z 401.3 [M+H]+
215 N-(4-chlorophenyl)-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine4,6-diamine 'H NMR (500 MHz, Acetone-rig) δ ppm 8.61 (1H, br. s.) 8.15 (1H, dd, 7=11.82, 7.72 Hz) 7.68 - 7.73 (2H, m) 7.38 - 7.50 (3 H, m) 6.66 (2H, br. s.) 2.80 (3H, s); MS m/z 405.2 [MHlj'
216 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-[2-(methoxymethyl)-1 H-benzimidazol-1 yl]pyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-rig) δ ppm 8.53 (1H, s) 8.13 - 8.17 (1H, m) 7.73 - 7.79 (2H, m) 7.64 - 7.69 (1H, m) 7.19 - 7.30 (4H, m) 6.82 - 7.13 (1H, m) 6.54 (2H, br. s.) 5.02 (2H, s) 3.28 (3H, s); MS m/z 431.3 [M+H]+
217 5-fluoro-2-[2-(methoxymethyl)-l H-benzimidazol-1-yl]-N-(4-methylphenyl)pyrimidine4,6-diamine ’H NMR (500 MHz, Acetone-rig) δ ppm 8.36 (1H, br. s.) 8.18 (1H, dd, 7=6.78, 1.73 Hz) 7.66 (1H, dd, 7=6.62, 1.89 Hz) 7.54 - 7.60 (2H, m) 7.17 - 7.30 (4H, m) 6.46 (2H, br. s.) 4.99 - 5.04 (2H, m) 3.28 (3H, s) 2.34 (3H, s); MS m/z 379.3 [M+H]+
154
WO 2014/081906
PCT/US2013/07U32
Cpd Name & Data
218 5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-(4-methoxyphenyl)pyrimidine4,6-diamine *H NMR (500 MHz, Acetone-^) δ ppm 8.31 (1H, br. s.) 8.14 - 8.19 (1H, m) 7.65 (1H, dd, 7=6.78, 1.73 Hz) 7.53 - 7.59 (2H, m) 7.25 (2H, quind, 7=7.41, 7.41, 7.41, 7.41, 1.58 Hz) 6.93 - 6.99 (2H, m) 6.43 (2H, br. s.) 4.97 - 5.02 (2H, m) 3.82 (3H, s); MS m/z 395.3 [M+H]+
219 N-(4-chlorophenyl)-5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]pyrimidine4,6-diamine ’Η NMR (500 MHz, Acetone-7rt) δ ppm 8.58 (1H, br. s.) 8.12-8.17 (1H, m) 7.73 - 7.79 (2H, m) 7.65 - 7.70 (1H, m) 7.37 - 7.41 (2H, m) 7.24 - 7.32 (2H, m) 6.58 (2H, br. s.) 5.03 (2H, s) 3.29 (3H, s); MS m/z 399.2 [M+H]+
220 5-fluoro-2-[2-(methoxymethyl)-1 H-benzimidazol-1-yl]-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine '11 NMR (500 MHz, Acetonc-7rt) δ ppm 8.83 (1H, br. s.) 8.11 - 8.18 (1H, m) 7.96 - 8.03 (2H, m) 7.66 - 7.73 (3H, m) 7.25 - 7.33 (2H, m) 6.68 (2H, br. s.) 5.05 (2H, s) 3.29 (3H, s); MS m/z 433.2 [M+H]+
222 l-(4-amino-5-fluoro-6-{[4-(trifluoromethyl)phenyl]amino}pyrimidin-2-yl)-2-methyl-lHbenzimidazole-6-carbonitrile 'll NMR (500 MHz, Acetone-70) δ ppm 8.91 (1H, s) 8.63 (1H, d, 7=1.58 Hz) 7.92 - 7.99 (2H, m) 7.74 (3H, t, 7=8.51 Hz) 7.61 (1H, dd, 7=8.20, 1.58 Hz) 6.84 (2H, br. s.) 2.90 (3H, s); MS m/z 428.3 [M+H]+
223 l-(4-amino-6-{[4-(difluoromethoxy)phenyl]amino}-5-fluoropyrimidin-2-yl)-2-methyl1 H-benzimidazole-6-carbonitrile ]H NMR (500 MHz, Acetone-^) δ ppm 8.58 - 8.63 (2H, m) 7.68 - 7.75 (3H, m) 7.57 7.62 (1H, m) 7.22 - 7.27 (2H, m) 6.84 - 7.16 (1H, m) 6.68 (2H, br. s.) 2.87 (3H, s); MS m/z 426.3 [M+H]+
224 1 - {4-amino-5-fluoro-6-[(4-methylphenyl)amino]pyrimidin-2-yl} -2-methyl-1Hbenzimidazole-6-carbonitrile ’ll NMR (500 MHz, Acetone^) δ ppm 8.61 (1H, s) 8.42 (1H, br. s.) 7.71 (1H, d, 7=8.20 Hz) 7.49 - 7.60 (3H, m) 7.24 (2H, d, 7=7.88 Hz) 6.58 (2H, br. s.) 2.87 (3H, s) 2.36 (3H, s); MS m/z 374.3 [M+H]+
225 l-{4-amino-5-fluoro-6-[(4-methoxyphenyl)amino]pyrimidin-2-yl}-2-methyl-lHbenzimidazole-6-carbonitrile ‘H NMR (500 MHz, Acetone-^) δ ppm 8.62 (1H, s) 8.37 (1H, s) 7.71 (1H, d, 7=8.20 Hz) 7.49 - 7.60 (3H, m) 6.98 - 7.03 (2H, m) 6.57 (2H, br. s.) 3.84 (3H, s) 2.84 (3H, s); MS m/z 390.3 [M+H]+
226 l-(4-amino-6-{[4-(difluoromethoxy)phenyl]amino}-5-fluoropyrimidin-2-yl)-2-methyllH-benzimidazole-5-carbonitrile 'Η NMR (500 MHz, Acctone-76) δ ppm 8.60 (1H, s) 8.28 (1H, dd, 7=8.51, 0.63 Hz) 8.00 (1H, dd, 7=1.58, 0.63 Hz) 7.70 - 7.77 (2H, m) 7.55 (1H, dd, 7=8.51, 1.58 Hz) 7.19 - 7.25 (2H, m) 6.98 (1H, t, 7=75.00 Hz) 6.63 (2H, br. s.) 2.83 (3H, s); MS m/z 426.3 [M+H]+
155
WO 2014/081906
PCT/US2013/071132
Cpd Name & Data
227 l-{4-amino-5-fluoro-6-[(4-methylphenyl)amino]pyrimidin-2-yl}-2-methyl-lHbenzimidazole-5-carbonitrile !H NMR (500 MHz, Acetone-/?) δ ppm 8.42 (1H, br. s.) 8.31 (1H, s) 7.99 (1H, s) 7.50 - 7.57 (3H, m) 7.20 (2H, d, /=8.20 Hz) 6.55 (2H, br. s.) 2.83 (3H, s) 2.34 (3H, s); MS m/z 374.3 [M+H]+
228 l-{4-amino-5-fluoro-6-[(4-methoxyphenyl)amino]pyrimidin-2-yl}-2-methyl-lHbenzimidazole-5-carbonitrile ’bl NMR (500 MHz, Acetone-/?) δ ppm 8.33 - 8.39 (1H, m) 8.29 (1H, d, /=8.51 Hz) 7.98 (1H, s) 7.49 - 7.56 (3H, m) 6.95 - 7.00 (2H, m) 6.51 (2H, br. s.) 3.83 (3H, s) 2.81 (3H, s); MS m/z 390.4 [M+H]+
229 l-(4-amino-5-fluoro-6-{[4-(trifluorornethyl)phenyl]amino}pyrimidin-2-yl)-2-methyl-lHbenzimidazole-5-carbonitrile 'H NMR (500 MHz, Acetone-^) δ ppm 8.90 (1H, s) 8.28 (1H, d, /=8.51 Hz) 8.02 (1H, s) 7.97 (2H, d, 7=8.51 Hz) 7.71 (2H, d, 7=8.20 Hz) 7.58 (1H, dd, /=8.51, 1.58 Hz) 6.78 (2H, br. s.) 2.87 (3H, s); MS m/z 428.3 [M+H]+
230 l-{4-amino-6-[(4-chlorophenyl)amino]-5-fluoropyrimidin-2-yl}-2-methyl-lHbenzimidazole-5-carbonitrile !H NMR (500 MHz, Acetone-/,?) δ ppm 8.64 (1H, br. s.) 8.28 (1H, dd, 7=8.51, 0.63 Hz) 8.01 (1H, d, /=1.58 Hz) 7.70 - 7.76 (2H, m) 7.57 (1H, dd, /=8.51, 1.58 Hz) 7.36 - 7.43 (2H, m) 6.67 (2H, br. s.) 2.84 (3H, s); MS m/z 394.2 [M+H]+
231 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-6-nitro-lH-benzimidazol-lyl)pyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-/^) δ ppm 9.02 (1H, d, /=2.84 Hz) 8.62 (1H, br. s.) 8.19 (1H, dd, /=8.83, 2.52 Hz) 7.71 - 7.77 (3H, m) 6.94 (1H, t, /=75.00 Hz) 6.68 (2H, s) 2.88 (3H, s); MS m/z 446.2 [M+H]+
232 5-fluoro-2-(2-methyl-6-nitro-1 H-benzimidazol-1 -yl)-N-(4-methylphenyl)pyrimidine-4,6diamine 2H NMR (500 MHz, Acetone-/?) δ ppm 9.03 (1H, d, /=2.84 Hz) 8.45 (1H, br. s.) 8.18 (1H, dd, /=8.83, 2.21 Hz) 7.74 (1H, d, /=8.83 Hz) 7.53 - 7.59 (2H, m) 7.18 (2H, d, /=7.88 Hz) 6.61 (2H, br. s.) 2.87 (3H, s) 2.32 (3H, s); MS m/z 394.2 [M+H]+
233 5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-6-nitro-1 H-benzimidazol-1 -yl)pyrimidine4,6-diamine '11 NMR (500 MHz, Acetone-/?) δ ppm 9.03 (1H, d, /=1.89 Hz) 8.38 (1H, br. s.) 8.17 (1H, dd, /=8.83, 2.21 Hz) 7.73 (1H, d, /=8.83 Hz) 7.52 - 7.60 (2H, m) 6.92 - 6.99 (2H, m) 6.57 (2H, br. s.) 3.80 (3H, s) 2.54 (3H, s); MS m/z 410.2 [M+H]+
236 5-fluoro-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-/?) δ ppm 9.04 (1H, d, /=2.52 Hz) 8.90 (1H, br. s.) 8.21 (1H, dt, /=8.83, 1.42 Hz) 7.99 (2H, dd, 7=8.35, 3.31 Hz) 7.77 (1H, d, /=8.83 Hz) 7.70 (2H, d, /=8.51 Hz) 6.83 (2H, br. s.) 2.92 (3H, s); MS m/z 448.2 [M+H]+
156
WO 2014/081906
PCT/US2013/071132
Cpd Name & Data
237 N-(4-chlorophenyl)-2-(4,6-difluoro-2-methyl-l H-benzimidazol-l-yl)-5-fluoropyrimi dine4,6-diamine *H NMR (500 MHz, Acetone-/?) δ ppm 8.62 (1H, br. s.) 7.79 (1H, dd, /=10.25, 2.05 Hz) 7.69 - 7.74 (2H, m) 7.37 - 7.44 (2H, m) 6.92 (1H, td, /=10.25, 2.21 Hz) 6.67 (2H, br. s.) 2.79 - 2.80 (3H, m); MS m/z 405.2 [M+H]+
238 2-(4,6-difluoro-2-methyl-l H-benzimidazol-1 -yl)-5-fluoro-N-[4(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-/?) δ ppm 8.69 (1H, s) 7.75 - 7.85 (3H, m) 7.36 (2H, d, /=8.20 Hz) 6.92 (1H, td, /=10.25, 2.52 Hz) 6.69 (2H, br. s.) 2.79 (3H, s); MS m/z 456.1 [M+H]+
240 N-(l,3-benzodioxol-5-yl)-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-/?) δ ppm 8.37 (1H, br. s.) 7.80 (1H, dd, /=9.46, 1.89 Hz) 7.20 (1H, d, /=2.21 Hz) 7.05 (1H, dd, /=8.35, 2.05 Hz) 6.84 - 6.92 (2H, m) 6.55 (2H, br. s.) 6.02 (2H, s) 2.79 (3H, s); MS m/z 416.2 [M+H]+
241 2-(4,6-difluoro-2-methyl-1 H-benzimidazol-1 -yl)-5-fluoro-N-(4-methylphenyl)pyrimidine4,6-diamine ]H NMR (500 MHz, Acetone-/?) δ ppm 8.41 (1H, br. s.) 7.80 (1H, dd, /=9.93, 2.36 Hz) 7.50 - 7.56 (2H, m) 7.20 (2H, d, /=8.20 Hz) 6.90 (1H, td, /=10.25, 2.52 Hz) 6.56 (2H, br. s.) 2.79 (3H, s) 2.34 (3H, s); MS m/z 386.2 [M+H]+
242 2-(4,6-difluoro-2-methyl-l H-benzimidazol-1-yl)-5-fluoro-N-(4methoxyphenyl)pyrimidine-4,6-diamine ’ll NMR (500 MHz, Acetone-/?) δ ppm 8.34 (1H, br. s.) 7.76 - 7.83 (1H, m) 7.47 - 7.55 (2H, m) 6.94 - 7.00 (2H, m) 6.89 (1H, td, /=10.25, 2.21 Hz) 6.52 (2H, br. s.) 3.82 (3H, s) 2.76 (3H, s); MS m/z 402.2 [M+H]+
243 2-(5,7-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 'H NMR (500 MHz, Acetone-/?) δ ppm 8.86 (1H, br. s.) 8.15 (1H, dd, /=11.66, 7.88 Hz) 7.91 - 7.98 (2H, m) 7.72 (2H, d, /=8.51 Hz) 7.48 (1H, dd, /=10.72, 7.57 Hz) 6.78 (2H, br. s.) 2.83 (3H, s); MS m/z 439.3 [M+H]+
244 5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-/?) δ ppm 8.82 (1H, br. s.) 8.00 (2H, d, /=8.51 Hz) 7.65 7.73 (3H, m) 7.45 (1H, d, /=8.51 Hz) 6.83 - 6.89 (1H, m) 6.67 (2H, br. s.) 3.64 - 3.69 (3H, m) 2.78 (3H, s); MS m/z 434.2 [M+H]+
245 N-(4-chlorophenyl)-5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)pyrimidine4,6-diamine *H NMR (500 MHz, Acetone-/?) δ ppm 8.57 (1H, br. s.) 7.74 - 7.79 (2H, m) 7.68 (1H, d, /=2.52 Hz) 7.44 (1H, d, /=8.51 Hz) 7.35 - 7.41 (2H, m) 6.85 (1H, dd, /=8.83, 2.52 Hz) 6.57 (2H, br. s.) 3.69 (3H, s) 2.75 (3H, s); MS m/z 399.2 [M+H]+
157
WO 2014/081906
PCT/US2013/071132
Cpd Name & Data
246 5-fluoro-2-(6-methoxy-2-methyl-1 H-benzimidazol-1 -yl)-N-[4(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-^) δ ppm 8.64 (1H, s) 7.84 - 7.89 (2H, m) 7.69 (1H, d, 7=2.21 Hz) 7.44 (1H, d, 7=8.83 Hz) 7.34 (2H, d, 7=8.20 Hz) 6.85 (1H, dd, 7=8.51, 2.52 Hz) 6.58 (2H, br. s.) 3.68 (3H, s) 2.75 (3H, s); MS m/z 449.2 [M+H]+
247 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-76) δ ppm 8.52 (1H, s) 7.74 - 7.79 (2H, m) 7.69 (1H, d, 7=2.52 Hz) 7.43 (1H, d, 7=8.51 Hz) 7.17 - 7.23 (2H, m) 6.81 - 7.12 (2H, m) 6.53 (2H, br. s.) 3.69 (3H, s) 2.74 (3H, s); MS m/z 432.2 [M+H]+
248 5-fluoro-2-(6-methoxy-2-methyl-1 H-benzimidazol-1 -yl)-N-(4-methylphenyl)pyrimidine4,6-diamine *H NMR (500 MHz, Acetone-74) δ ppm 8.34 (1H, br, s) 7.70 (1H, d, 7=2.52 Hz) 7.56 - 7.60 (2H, m) 7.42 (1H, d, 7=8.83 Hz) 7.17 (2H, d, 7=8.20 Hz) 6.83 (1H, dd, 7=8.83, 2.52 Hz) 6.45 (2H, br. s.) 3.65 (3H, s) 2.75 (3H, s) 2.33 (3H, s); MS m/z> 380.2 [M+H]+
249 5-fluoro-2-(6-methoxy-2-methyl-1 H-benzimidazol-1 -yl)-N-(4methoxyphenyl)pyrimidine-4,6-diamine 'H NMR (500 MHz, Acetone-dQ δ ppm 8.27 (1H, br. s.) 7.70 (1H, d, 7=2.52 Hz) 7.54 - 7.60 (2H, m) 7.38 - 7.43 (1H, m) 6.92 - 6.97 (2H, m) 6.82 (1H, dd, 7=8.51, 2.52 Hz) 6.41 (2H, br. s.) 3.82 (3H, s) 3.67 (3H, s) 2.72 (3H, s); MS m/z 396.2 [M+H]+
250 N-( 1,3-benzodioxol-5-yl)-5-fluoro-2-(6-methoxy-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine T-I NMR (500 MHz, Acetone-d6) δ ppm 8.32 (1H, br. s.) 7.71 (1H, d, 7=2.52 Hz) 7.42 (1H, d, 7=8.51 Hz) 7.30 - 7.33 (1H, m) 7.09 (1H, dd, 7=8.35, 2.05 Hz) 6.81 - 6.87 (2H, m) 6.44 (2H, br. s.) 6.01 (2H, s) 3.72 (3H, s) 2.74 (3H, s); MS m/z 409.2 [M+H]+
254 5-fluoro-2-(2-methyl-5-nitro-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6diamine 'H NMR (500 MHz, Acetone-d6) δ ppm 8.45 - 8.49 (1H, m) 8.44 (1H, d, 7=1.89 Hz) 8.31 (1H, d, 7=9.14 Hz) 8.11 (1H, dd, 7=8.98, 2.36 Hz) 7.54 - 7.57 (2H, m) 7.21 (2H, d, 7=8.20 Hz) 6.59 (2H, br. s.) 2.85 (3H, s) 2.34 (3H, s); MS m/z 394.2 [M+H]+
255 5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-5-nitro-lH-benzimidazol-l-yl)pyrimidine4,6-diamine ’H NMR (500 MHz, Acetone-dQ δ ppm 8.43 (1H, d, 7=1.89 Hz) 8.40 (1H, br. s.) 8.30 (1H, d, 7=9.14 Hz) 8.10 (1H, dd, 7=8.99, 2.36 Hz) 7.52 - 7.57 (2H, m) 6.96 - 7.01 (2H, m) 6.55 (2H, br. s.) 3.83 (3H, s) 2.83 (3H, s); MS m/z 410.2 [M+H]+
256 2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine- 4,6-diamine ’H NMR (500 MHz, Acetone-dQ δ ppm 8.25 (1H, s) 7.53 - 7.59 (2H, m) 7.42 (1H, d, 7=1.58 Hz) 7.24 (1H, d, 7=8.83 Hz) 6.93 - 6.99 (2H, m) 6.61 (1H, dd, 7=8.20, 2.21 Hz) 6.33 (2H, s) 4.30 (2H, br. s.) 3.81 (3H, s) 2.67 (3H, s); MS m/z 380.3 [M+H]+
158
WO 2014/081906
PCT/US2013/071132
Cpd Name & Data
257 2-(6-amino-2-methyl-l H-benzimidazol- l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine ‘H NMR (500 MHz, Acetone-^) δ ppm 8.48 (1H, br. s.) 7.75 - 7.82 (2H, m) 7.42 (1H, d, 7=2.21 Hz) 7.25 (1H, d, 7=8.20 Hz) 7.17 - 7.22 (2H, m) 6.96 (1H, t, 7=75.00 Hz) 6.64 (1H, dd, 7=8.51, 2.21 Hz) 6.44 (2H, br. s.) 4.36 (2H, s) 2.68 (3H, s); MS m/z 416.2 [M+H]+
258 2-(6-amino-2-m ethyl-1 H-benzimidazol-1 -yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6diamine JH NMR (500 MHz, Acetone-76) δ ppm 8.15 (1H, br. s.) 7.39 - 7.46 (2H, m) 7.28 (1H, d, 7=2.21 Hz) 7.09 (1H, d, 7=8.20 Hz) 7.04 (2H, d, 7=8.20 Hz) 6.47 (1H, dd, 7=8.51, 2.21 Hz) 6.22 (2H, br. s.) 4.16 (2H, s) 2.54 (3H, s) 2.18 (3H, s); MS m/z 364.3 [M+H]+
259 N-(4-chlorophenyl)-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine ’Η NMR (500 MHz, Acetone-7,) δ ppm 8.60 (1H, br. s.) 8.13 (1H, dd, 7=9.46, 5.04 Hz) 7.71 - 7.78 (2H, m) 7.36 - 7.43 (2H, m) 7.29 (1H, dd, 7=9.30, 2.36 Hz) 6.99 (1H, td, 7=9.30, 2.52 Hz) 6.60 (2H, br. s.) 2.80 (3H, s); MS m/z 387.2 [M+H]+
260 N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone^) δ ppm 8.76 (1H, br. s.) 8.13 (1H, dd, 7=8.83, 5.04 Hz) 7.86 (1H, dd, 7=11.98, 2.52 Hz) 7.54 - 7.59 (1H, m) 7.45 - 7.51 (1H, m) 7.30 (1H, dd, 7=9.30, 2.36 Hz) 7.02 (1H, td, 7=9.22, 2.68 Hz) 6.69 (2H, br. s.) 2.84 (3H, s); MS m/z 405.2 [M+H]+
261 N-(4-chloro-3 -fluorophenyl)-5 -fluoro-2-(2 -methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6diamine *H NMR (500 MHz, Acetone^) δ ppm 8.74 (1H, br. s.) 8.11 (1H, dd, 7=7.57, 1.89 Hz) 7.90 (1H, dd, 7=11.98, 2.52 Hz) 7.58 (2H, td, 7=7.88, 2.21 Hz) 7.47 (1H, t, 7=8.67 Hz) 7.18 - 7.28 (2H, m) 6.65 (2H, br. s.) 2.82 (3H, s); MS m/z 387.2 [M+H]+
262 N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-l H-benzimidazol-1yl)pyrimidine-4,6-diamine JH NMR (500 MHz, Acetone^) δ ppm 8.77 (1H, br. s.) 7.93 (1H, dd, 7=10.09, 2.21 Hz) 7.83 (1H, dd, 7=11.82, 2.36 Hz) 7.53 - 7.59 (2H, m) 7.46 - 7.51 (1H, m) 7.05 (1H, td, 7=9.14, 2.52 Hz) 6.72 (2H, br. s.) 2.82 (3H, s); MS m/z 405.2 [M+H]+
270 2-(2-ethyl-l H-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-7>) δ ppm 8.36 (1H, br. s.) 8.07 - 8.11 (1H, m) 7.54 - 7.62 (3H, m) 7.15 - 7.24 (4H, m) 6.46 (2H, br. s.) 3.26 (2H, q, 7=7.46 Hz) 2.33 (3H, s) 1.30 1.33 (3H, m); MS m/z 363.3 [M+H]+
271 2-(2-ethyl-l H-benzimidazol- l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-diamine 'H NMR (500 MHz, Acetone-JQ δ ppm 8.15 (1H, br. s.) 7.93 - 7.97 (1H, m) 7.39 - 7.46 (3H, m) 6.99 - 7.10 (2H, m) 6.78 - 6.83 (2H, m) 6.28 (2H, s) 3.68 (3H, s) 3.10 (2H, q, 7=7.36 Hz) 1.14- 1.17 (3H,m); MS m/z 379.3 [M+H]+
159
WO 2014/081906
PCT/US2013/071132
Cpd Name & Data
272 2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethoxy)phenyl]pyrimidine4,6-diamine 'll NMR (500 MHz, Acetone®) δ ppm 8.67 (1H, s) 8.04 - 8.10 (1H, m) 7.80 - 7.87 (2H, m) 7.58 - 7.64 (1H, m) 7.33 (2H, d, 7=8.20 Hz) 7.14 - 7.26 (2H, m) 6.60 (2H, s) 3.26 (2H, q, 7=7.36 Hz) 1.31 - 1.34 (3H, m); MS m/z 433.2 [M+H]+
273 N-(l,3-benzodioxol-5-yl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine *H NMR (500 MHz, Acetone®) δ ppm 8.32 (1H, br. s.) 8.08 - 8.13 (1H, m) 7.58 (1H, d, 7=7.57 Hz) 7.28 (1H, d, 7=1.89 Hz) 7.15 - 7.24 (2H, m) 7.07 (1H, dd, 7=8.67, 2.05 Hz) 6.85 (1H, d, 7=8.51 Hz) 6.40 - 6.48 (2H, m) 6.01 (2H, s) 3.25 (2H, q, 7=7.57 Hz) 1.30 1.33 (3H, m); MS m/z 393.2 [M+H]+
274 N-(4-chlorophenyl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine ’ll NMR (500 MHz, Acetone®) δ ppm 8.57 (1H, br. s.) 8.03 - 8.09 (1H, m) 7.72 - 7.79 (2H, m) 7.60 (1H, d, 7=7.57 Hz) 7.34 - 7.40 (2H, m) 7.16 - 7.26 (2H, m) 6.56 (2H, br. s.) 3.26 (2H, q, 7=7.57 Hz) 1.33 (3H, t, 7=7.57 Hz); MS m/z 383.4 [M+H]+
275 N-(4-chloro-3-fluorophenyl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine !H NMR (500 MHz, Acetone®) δ ppm 8.75 (1H, br. s.) 8.06 (1H, d, 7=6.94 Hz) 7.90 (1H, dd, 7=11.98, 2.52 Hz) 7.62 (1H, dd, 7=6.94, 1.58 Hz) 7.54 - 7.58 (1H, m) 7.42 - 7.49 (1H, m) 7.18 - 7.29 (2H, m) 6.65 (2H, br. s.) 3.29 (2H, q, 7=7.36 Hz) 1.36 (3H, t, 7=7.41 Hz); MS m/z 401.4 [M+H]+
276 2-(2-cyclopropyl-l H-benzimidazol-1 -yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6diamine ’Η NMR (500 MHz, Acetone®) δ ppm 8.36 (1H, br. s.) 8.02 - 8.06 (1H, m) 7.61 - 7.67 (2H, m) 7.46 - 7.53 (1H, m) 7.12 - 7.23 (4H, m) 6.47 (2H, br. s.) 3.01 - 3.10 (1H, m) 2.32 (3H,s) 1.16-1.21 (2H,m) 0.98 (2H,dq, 7=8.47, 3.38 Hz); MS m/z 375.4 [M+H]+
277 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6diamine JH NMR (500 MHz, Acetone®) δ ppm 8.29 (1H, br. s.) 8.04 (1H, d, 7=8.83 Hz) 7.58 7.65 (2H, m) 7.46 - 7.51 (1H, m) 7.10 - 7.21 (2H, m) 6.89 - 6.96 (2H, m) 6.43 (2H, br. s.) 3.81 (3H, s) 3.02 - 3.10 (1H, m) 1.13-1.18 (2H, m) 0.96 (2H, dq, 7=8.35, 3.42 Hz); MS m/z 391.3 [M+H]+
278 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone®) δ ppm 8.65 (1H, s) 7.98 - 8.03 (1H, m) 7.87 - 7.93 (2H, m) 7.49 - 7.54 (1H, m) 7.31 (2H, d, 7=8.20 Hz) 7.12 - 7.24 (2H, m) 6.60 (2H, br. s.) 2.98 3.05 (1H, m) 1.17 - 1.23 (2H, m) 0.95 - 1.02 (2H, m); MS m/z 445.3 [M+H]+
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Cpd Name & Data
279 N-(4-chlorophenyl)-2-(2-cyclopropyl-l H-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine ’H NMR (500 MHz, Acetone» δ ppm 8.59 (1H, br. s.) 7.97 - 8.04 (1H, m) 7.80 - 7.86 (2H, m) 7.47 - 7.55 (1H, m) 7.32 - 7.38 (2H, m) 7.12 - 7.23 (2H, m) 6.58 (2H, br. s.) 2.96 - 3.05 (1H, m) 1.17 - 1.25 (2H, m) 0.97 - 1.04 (2H, m); MS m/z 395.3 [M+H]+
280 N-(4-chloro-3-fluorophenyl)-2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine *Η NMR (500 MHz, Acetone» δ ppm 8.77 (1H, br. s.) 7.96 - 8.06 (2H, m) 7.60 (1H, dd, >7.88, 2.52 Hz) 7.53 (1H, d, >6.94 Hz) 7.45 (1H, t, >8.67 Hz) 7.16 - 7.25 (2H, m) 6.68 (2H, br. s.) 2.96 - 3.03 (1H, m) 1.21 - 1.26 (2H, m) 1.02 - 1.07 (2H, m); MS m/z 413.3 [M+H]+
281 5-fluoro-2-(5-fluoro-2-methyl-1 H-benzimidazol-1 -yl)-N-(4-methylphenyl)pyrimidine-4,6diamine 1H NMR (500 MHz, Acetone») δ ppm 8.39 (1H, br. s.) 8.15 (1H, dd, J=8.51, 5.04 Hz) 7.53 - 7.58 (2H, m) 7.27 (1H, dd, J=9.62, 2.36 Hz) 7.19 (2H, d, >8.20 Hz) 6.92 - 7.00 (1H, m) 6.51 (2H, br. s.) 2.79 (3H, s) 2.34 (3H, s); MS m/z 367.3 [M+H]+
282 5-fluoro-2-(5-fluoro-2-methyl-1 H-benzimidazol-1 -yl)-N-(4-methoxyphenyl)pyrimidine4,6-diamine ’H NMR (500 MHz, Acetone» δ ppm 8.30 (1H, br. s.) 8.14 (1H, dd, >9.30, 4.89 Hz) 7.51 - 7.58 (2H, m) 7.26 (1H, dd, >9.46, 2.52 Hz) 6.91 - 7.00 (3H, m) 6.44 (2H, br. s.) 3.83 (3H, s) 2.76 (3H, s); MS m/z 383.3 [M+H]+
283 5-fluoro-2-(5-fluoro-2-methyl-1 H-benzimidazol-1-yl)-N-[4(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine 'H NMR (500 MHz, Acetone» δ ppm 8.66 (1H, s) 8.12 (1H, dd, >8.67, 4.89 Hz) 7.80 - 7.86 (2H, m) 7.35 (2H, d, >8.20 Hz) 7.29 (1H, dd, >8.83, 2.52 Hz) 6.97 (1H, td, >9.30, 2.52 Hz) 6.62 (2H, s) 2.79 (3H, s); MS m/z 437.3 [M+H]+
284 2-(6-amino-2-methyl-1 H-benzimidazol-1-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-di amine Ή NMR (500 MHz, Acetone» δ ppm 7.86 (2H, d, >8.51 Hz) 7.53 (2H, d, >8.51 Hz) 7.28 (1H, d, >2.21 Hz) 7.13 (1H, d, >8.51 Hz) 6.50 (1H, dd, >8.51, 2.21 Hz) 6.42 (2H, br. s.) 4.26 (2H, s) 2.56 (3H, s) MS m/z 418.3 [M+H]+
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Example 11
5-fluoro-N-(4-methoxyphenyl)-2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)pyrimidine-4,6diamine (Cpd 239)
Cl
Figure AU2013348009C1_D0177
NaOH
Figure AU2013348009C1_D0178
Step 1. To a mixture of 1 -aminopyridinium iodide (9.59 g, 43.2 mmol) and methyl but-2-ynoate (5.2mL, 51.83 mmol) in DMF (50 mL) at 0°C was added K2CO3 (11.94g, 86.4 mmol). The reaction mixture was warmed to room temperature and stirred for 3 days until UPLC showed complete conversion to product. The reaction mixture was partitioned between water and EtOAc. The organic phase was concentrated, then MeOH (50 mL) and NaOH (6 mL, 50% in H2O) were added and the reaction mixture was heated at 70°C for 1 hour. The MeOH was evaporated and the remaining mixture was acidified with IN HC1 to about pH 4. A crude 2-methylpyrazolo[l,5-a]pyridine-3-carboxylic acid was isolated on a filter and dried under vacuum, then dissolved in MeOH (50 mL) and CHCI3 (100 mL) and Niodosuccinimide (7.3g, 32.4 mmol) were added in one portion. The reaction mixture was stirred for 20 minutes at room temperature. The MeOH was evaporated and the remainder was washed three times with an aqueous NaHCO3 solution. The organic phase was dried over Na2SO4, the solvent was removed under reduced pressure, and the crude product was purified by silica gel chromatography to give 3-iodo-2-methylpyrazolo[l,5-a]pyridine (4.2 g, 38% for 3 steps) as an off-white solid.
!H NMR (500 MHz, Acetone-ri^ δ ppm 8.51 (dt, J = 6.8, 1.3 Hz, 1H), 7.41 (dt, J = 8.8, 1.3 Hz, 1H), 7.31 (ddd, J = 8.8, 6.8, 1.3 Hz, 1H), 6.90 (td, J = 6.8, 1.3 Hz, 1H), 2.42 (s, 3H); MS m/z 298.1 [M+H]+.
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Step 2. To a solution of 3-iodo-2-methylpyrazolo[l,5-a]pyridine (340 mg,l .32 mmol) in dry THF (10 mL) at 0°C was added an isopropylmagnesium chloride lithium chloride complex solution (iPrMgCl.LiCl) (1.5 mL, 1.97 mL). The reaction mixture was stirred at 0°C for 30 minutes and 4,6-dichloro-5-fluoro-2-(methylsulfonyl)pyrimidine (484 mg, 1.97 mmol) in dry THF (20 mL) was added. The reaction mixture was stirred at 0°C for 1 hour, and the reaction was quenched with water. The crude product was extracted with CH2CI2 three times. The combined organic extracts were washed with brine, then dried over Na2SO4, concentrated, and triturated in CH3CN (10 mL). The resulting precipitate was filtered and dried providing 3-(4,6-dichloro-5-fluoropyrimidin-2-yl)-2-methylpyrazolo[l,5ajpyridine (270 mg, 68%) isolated as a tan solid.
*H NMR (500 MHz, DMSO-cA) δ ppm 8.79 (d, J = 6.9 Hz, 1H), 8.34 (d, J = 8.8 Hz, 1H), 7.61 (ddd, J = 8.8, 6.9, 0.9 Hz, 1H), 7.13 (td, J = 6.9, 1.1 Hz, 1H), 2.70 (s, 3H). MS m/z 298.1 [M+H]+.
Step 3. 3-(4,6-Dichloro-5-fhioropyrimidin-2-yl)-2-methylpyrazolo[l,5-a]pyridine (65 mg, 0.21 mmol) and 4-methoxyaniline (52 mg, 0.42 mmol) were mixed in EtOH (1 mL) and heated in a sealed tube at 100°C until UPLC showed complete conversion (3 hours). After the starting materials were consumed, the reaction was cooled to room temperature and diluted with water (5 mL) to precipitate the product. The product was collected by filtration, washed with water and subsequently washed with hexanes. The crude product, without drying, was dissolved in iPrOAc (2 mL), then saturated ammonia in water (150 pL) was added. The reaction mixture was heated at 100°C in a sealed tube for 24 hours until UPLC showed complete consumption of starting material. A crude product was precipitated by addition of water (10 mL), then filtered and purified by chromatography on silica gel to provide the title compound (26 mg, 34 % in two steps).
’Η NMR (500 MHz, Acetone-^) δ ppm 8.54 (dt, J = 8.9, 1.2 Hz, 1H), 8.47 (dt, J = 6.9, 1.1 Hz, 1H), 7.93 (br. s„ 1H), 7.59 (dd, J = 6.6, 2.2 Hz, 2H), 7.21 (ddd, J = 9.0, 6.8, 0.9 Hz, 1H), 6.98 (dd, J = 6.6, 2.2 Hz, 2H), 6.87 (td, J = 6.8, 1.3 Hz, 1H), 5.96 (br. s., 2H), 2.84 (s, 3H), 2.70 (s, 3H); MS m/z 383.2 [M+H]+.
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Additional compounds of Formula (I) or a form thereof described herein may be
prepared according to the procedure of Example 11 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
173 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methylpyrazolo[l,5-a]pyridin-3yl)pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-^) δ ppm 8.55 (dt, J = 8.9, 1.2 Hz, 1H), 8.49 (dt, J = 6.9, 1.0 Hz, 1H), 8.20 (br. s„ 1H), 7.76 - 7.81 (m, 2H), 7.20 - 7.27 (m, 3H), 6.98 (t, J = 75 Hz, 1H) 6.89 (td, J = 6.9, 1.4 Hz, 1H), 6.08 (br. s, 2H), 2.72 (s, 3H); MS m/z 401.2 [M+H]+
177 5-fhioro-2-(2-methylpyrazolo[ 1,5-a]pyridin-3-yl)-N-[4(trifhioromethyl)phenyl]pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-^) δ ppm 8.44 (dt, J = 9.1, 1.1 Hz, 1H), 8.37 (dt, J = 6.9, 0.9 Hz, 1H), 8.39 (br. s., 1H), 7.87 (d, J = 8.5 Hz, 2H), 7.55 (d, J = 8.5 Hz, 2H), 7.13 (ddd, J = 9.1, 6.7, 1.3 Hz, 1H), 6.77 (td, J = 6.8, 1.6 Hz, 1H), 6.09 (br. s., 2H), 2.62 (s, 3H); MS m/z 403.4 [M+H]+
178 5-fluoro-2-[6-fluoro-2-(triiluoromethyI)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine Ή NMR (500 MHz, Acetone-^) δ ppm 8.76 - 8.81 (m, 1H), 8.70 (br. s., 1H), 7.91 (d, J = 8.5 Hz, 2H), 7.68 (dd, J = 10.1, 4.7 Hz, 1H), 7.47 (d, J = 8.5 Hz, 2H), 7.45 (t, J = 9.8 Hz, 1H), 6.52 (br. s., 2H); MS m/z 475.3 [M+H]+
Example 12
2-(2-cyclopropylpyrazolo[l,5-a]pyridin-3-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine (Cpd 180)
Figure AU2013348009C1_D0179
Figure AU2013348009C1_D0180
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Step 1. To a solution of cyclopropylacetylene (777.0 mg, 9.82 mmol) in THF (5 mL) at -78°C was added an isopropylmagnesium chloride lithium chloride complex solution (9.0 mL, 1.3 M in THF) dropwise. The mixture was warmed to 0°C and stirred for 30 minutes. To the mixture at -78°C was added 4,6-dichloro-5-fluoro-2-(methylsulfonyl)pyrimidine (4.80 g, 19.6 mmol), then the mixture was warmed to 0°C and stirred for 1 hour. The mixture was partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSO4, then filtered and evaporated. The residual material was separated by silica gel column chromatography (eluting with 1:9 ethyl acetate-hexane) to afford 4,6-dichloro-2(cyclopropylethynyl)-5-fluoropyrimidine (1.17 g, 45%).
'H NMR (500 MHz, Acetone-/) δ ppm 1.53 - 1.67 (m, 1H), 0.98 - 1.10 (m, 2H), 0.83 - 0.94 (m, 2H); MS m/z 231.1 (100) [M+H]+.
Step 2. A mixture of 4,6-dichloro-2-(cyclopropylethynyl)-5-fluoropyrimidine (241.0 mg, 1.04 mmol) and 4-difluoromethoxy aniline (707.0 mg, 4.45 mmol) in EtOH (2 mL) was stirred at reflux for 1 hour. After cooling, the mixture was partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSO4, then filtered and evaporated. The residual material was separated by silica gel column chromatography (eluting with 1:20 and 1:10 ethyl acetate-hexane) to afford 6-chloro-2-(cyclopropylethynyl)N-(4-(difluoromethoxy)phenyl)-5-fluoropyrimidin-4-amine (258.0 mg, 70%); MS m/z 354.2 (100) [M+H]+, 356.2 (40).
Step 3. To 6-chloro-2-(cyclopropylethynyl)-/V-(4(difluoromethoxy)phenyl)-5fluoropyrimidin-4-amine was added DMSO (2 mL) and NH4OH (27%, 0.1 mL). The reaction mixture was sealed and stirred at 100°C for 2 days. The reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed with water (2 x 20 mL) and brine, dried over MgSO4, then filtered and evaporated. The residual material was separated by silica gel column chromatography (eluting with 1:4 ethyl acetate-hexane) to afford 2-(2-cyclopropylpyrazolo[l,5-a]pyridin-3-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine (149.0 mg, 64%). MS m/z 335.5 (80) [M+H]\ 336.2 (100).
Step 4. A mixture of 2-(2-cyclopropylpyrazolo[l ,5-a]pyridin-3-yl)-N-[4(difluoromethoxy)phenyl]-5-fluoropyrimidine-4,6-diamine (100.0 mg, 0.30 mmol), pyridinium-1-ylazanide (74.0 mg, 0.30 mmol), K2CO3 (43.0 mg, 0.31 mmol) and DMF (2 mL) was stirred at room temperature for 1 day, and then at 80°C for 1 day. The reaction mixture was partitioned between ethyl acetate and water. The organic phase was washed
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'll NMR (500 MHz, Acetone-i/d) δ ppm 8.55 (d, J= 8.83 Hz, 1H), 8.41 (d, 7= 6.94 Hz, 1H). 8.20 (br. s„ 1H), 7.63 - 7.91 (m, 2H), 7.21 (ddd, 7= 0.95, 6.78, 8.98 Hz, 1H), 7.17 (d, 7 = 8.83 Hz, 2H), 6.80 - 7.10 (t, J = 75.00 Hz, 1H), 6.86 (dt, J= 1.26, 6.78 Hz, 1H), 6.10 (br. s., 2H), 3.44 (m, 1H), 0.53 - 1.13 (m, 4H); MS m/z 427.3 (100) [M+H]+, 428.3 (50).
Example 13 [3-(4-amino-6- {[4-(difhioromethoxy)phenyl]amino}-5-fluoropyrimidin-2-yl)-5fluoropyrazolo[l,5-a]pyridin-2-yl]mcthanol (Cpd 181)
Figure AU2013348009C1_D0181
PdCI2(ACN)2,
XPhos,
Figure AU2013348009C1_D0182
Figure AU2013348009C1_D0183
Figure AU2013348009C1_D0184
Figure AU2013348009C1_D0185
Figure AU2013348009C1_D0186
Figure AU2013348009C1_D0187
F F
Step 1. A mixture of 2-chloro-4-fluoropyridine (2.19 g, 16.65 mmol), prop-2-yn-
1- ol (1.86 g, 33.29 mmol), bis(acetonitrile)dichloropalladium(II) (215.6 mg, 0.83 mmol) and
2- dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl (Xphos) (794.3 mg, 0.17 mmol) in
NMP (15 mL) was degassed by three cycles of vacuum pumping and N2 purging, and then
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Step 2-4. To a solution of 3-(4-fluoropyridin-2-yl)prop-2-yn-l-ol (820.0 mg, 5.43 mmol) in dichloromethane (10 mL) was added 2-[(aminooxy)sulfonyl]-l,3,5trimethylbenzene (1.5 g, 6.98 mmol) portion wise at 0°C. The resulting mixture was stirred at ambient temperature for 2 days. The solvent removed under a blowing N2 stream to give a crude mixture. To the crude mixture in DMF (3 mL) was added K2CO3 (825.0 mg, 5.97 mmol) at 0°C. The resulting mixture was stirred at room temperature for 24 hours, and then partitioned between ethyl acetate and water. The organic phase was washed with water and brine, dried over MgSO4, then filtered and evaporated. The residual material was used in the next step without further purification.
A mixture of crude material, A-iodosuccinimidc (1.2 g, 5.33 mmol) in chloroform (10 mL) was stirred at ambient temperature for 2 hours, and then partitioned between ethyl acetate and water. The organic phase was washed with water and brine, dried over MgSO4, then filtered and evaporated. The residual material was separated by silica gel column chromatography (eluting with 1:1 dichloromethane:hexane, then 1% methanol in 1:4 ethyl acetaterdichloromethane to afford (5-fluoro-3-iodopyrazolo[l,5-a]pyridin-2-yl)methanol as an oil (1.4 g, 50%).
Step 5. To a solution of (5-fluoro-3-iodopyrazolo[l,5-a]pyridin-2-yl)methanol (500.0 mg, 1.71 mmol) in dichloromethane (3 mL) was added imidazole (139.5 mg, 2.05 mmol), followed by tert-butyldimethylsilyl chloride (384.0 mg, 2.55 mmol) in dichloromethane (5 mL) added dropwise at 0°C. The resulting mixture was stirred at ambient temperature for 30 minutes, then filtered through a pad of silica gel/selite, washing with dichloromethane to provide 2-[(z‘er/-butyldimethylsilyloxy)methyl]-5-fluoro-3iodopyrazolo[l,5-a]pyridine (470,0 mg, 72%).
Step 6. To a solution of 2-[(tert-butyldimethylsilyloxy)methyl]-5-fluoro-3iodopyrazolo[l,5-<7]pyridine (470.0 mg, 1.15 mmol) in THF (5 mL) was added an isopropylmagnesium chloride lithium chloride complex solution (1.07 mL, 1.3 M in THF) at
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-78°C dropwise. The mixture was warmed to 0°C and stirred for 30 minutes, and then 4,6dichloro-5-fluoro-2-(methylsulfonyl)pyrimidine (4.80 g, 19.6 mmol) was added in one portion at -78°C. The mixture was stirrrd at 0°C for 1 hour and then partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSCfi, then filtered and evaporated. The residual material was separated by silica gel column chromatography (eluting with 1:9 ethyl acetate:hexane) to afford 2-[(/ertbutyldimethylsilyloxy)methyl]-3-(4,6-dichloro-5-fluoropyrimidin-2-yl)-5-fluoropyrazolo[l,5/pyridine (205.0 mg, 40%).
Steps 7-8. Amixtureof2-[(/<?r/-butyldimethylsilyloxy)methyl]-3-(4,6-dichloro-5fluoropyrimidin-2-yl)-5-fluoropyrazolo[l,5-/pyridine (102.0 mg, 0.23 mmol), 4difluoromethoxy aniline (145.0 mg, 0.92 mmol) and ethanol (1 mL) was heated at 90°C overnight. After cooling, the mixture was poured into ice-water to afford a solid. The solid was collected by filtration, followed by washing with water and hexane. The solid was dried under the vacuum to provide 2-[2-[(ter/-butyldimethylsilyloxy)methyl]-5-fluoropyrazolo[l,5a]pyridin-3-yl]-6-chloro-A-(4-difluoromethoxy)phenyl]-5-fluoropyrimidin-4-amine (a mixture of TBS protected and unprotected product).
To the dried solid was added DMSO (3 mL) and NH4OH (0.3 mL). The reaction mixture was sealed and stirred at 100°C for 2 days. The mixture was partitioned between ethyl acetate and water and the organic phase was washed with water (2x10 mL) and brine, dried over MgSCfi, then filtered and evaporated. The residual material was separated by silica gel column chromatography (eluting with 1-5 % methanol in dichloromethane) to provide the title compound as a white solid (25.0 mg, 25 % for two steps); m.p. 198 - 200°C. ’Η NMR (500 MHz, Acetone-/,) δ ppm 8.50 - 8.64 (m, 1H), 8.35 (s, 1H), 8.06 - 8.21 (m, 1H), 7.64 (d, <7 = 8.83 Hz, 2H), 7.24 (d, J= 8.83 Hz, 2H), 6.80 - 7.10 (t, J = 75.00 Hz, 1H), 6.86 - 6.93 (m, 1H), 6.23 - 6.41 (m, 2H), 5.46 - 5.66 (m, 1H), 4.68 - 4.83 (m, 2H); MS m/z 435.2 (100) [M+H]+, 436.2 (20).
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Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 13 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
186 N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-5-fluoropyrazolo[l,5-a]pyridin-3-yl)-5fluoropyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-dg) δ ppm 8.54 (dd, J= 5.20, 7.41 Hz, 1H), 8.25 (dd, J = 2.68, 10.88 Hz, 1H), 8.18 (br. s., 1H), 7.71 (d, J= 9.14 Hz, 2H), 7.21 (d, 9.14 Hz, 2H), 6.80 - 7.10 (t, J = 75.00 Hz, 1H), 6.76 - 6.88 (m, 1H), 6.14 (br. s., 2H), 3.24 (q, J= 7.57 Hz, 2H), 1.20 - 1.35 (m, 3H); m.p. 103-105 °C; MS m/z 433.6 [M+H]+
187 2-(2-ethyl-5-fluoropyrazolo[l,5-a]pyridin-3-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine !H NMR (500 MHz, Acetone-d6) δ ppm 8.53 - 8.59 (m, 1H), 8.50 (br. s„ 1H), 8.28 (dd, J = 2.68, 10.25 Hz, 1H), 7.93 (d, J= 8.51 Hz, 2H), 7.69 (d, J= 8.51 Hz, 2H), 6.83 (dt, J= 2.99, 7.33 Hz, 1H), 6.28 (br. s., 2H), 3.28 (q, J= 7.46 Hz, 2H), 1.28 (t, J= 7.57 Hz, 3H); m.p. 164-166 °C; MS m/z 435.2 [M+H]+
188 N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-5-fluoropyrazolo[l,5-a]pyridin-3-yl)5 - fluoropyrimidine-4,6-diamine ’H NMR (500 MHz, Acetone-dg) δ ppm 8.49 - 8.64 (m, 1H), 8.33 - 8.40 (m, 1H), 8.24 8.32 (m, 1H), 7.77 - 7.85 (m, 1H), 7.44 - 7.50 (m, 1H), 7.29 - 7.38 (m, 1H), 6.80 - 7.10 (t, J = 75.00 Hz, 1H), 6.81 - 6.87 (m, 1H), 6.17 - 6.34 (m, 2H), 3.27 (d, J= 7.57 Hz, 2H), 1.28 (t, J= 7.57 Hz, 3H); m.p. 150-152 °C; MS m/z 452. [M+H]+
Example 14
5-fluoro-2-(2-methylimidazo[ 1,2-a]pyridin-3 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine (Cpd 169)
Figure AU2013348009C1_D0188
POCI3
Figure AU2013348009C1_D0189
Figure AU2013348009C1_D0190
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Step 1. To a solution of 2-methylimidazo[l,2-a]pyridine-3-carboximidamide pivaloate (250 mg, 0.905 mmol) and dimethyl 2-fluoromalonate (272 mg, 1.81 mmol) in MeOH (5 mL) was added 30% NaOMe in MeOH (0.2 mL). The mixture was heated at 85°C in a sealed tube for 72 hours until UPLC showed complete consumption of the starting material. The reaction mixture was concentrated under reduced pressure, then diluted with water (5 mL), and acidified with IN HC1 to about pH 7. A tan precipitate was collected by filtration giving 5-fluoro-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6-diol. 5fluoro-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6-diol (180 mg, 76%). The product (180 mg, 0.69 mmol) was mixed with phosphorus oxychloride (3 mL) in a microwave vial, then the vial was sealed and microwaved for 15 minutes at 150°C. The reaction mixture was transferred into a 25 mL round-bottom flask and concentrated under reduced pressure. The remainder was redissolved in EtOAc (10 mL) and washed with an aqueous NaHCO3 solution three times. The organic phase was dried over Na^SCfi, then filtered and evaporated to afford 3-(4,6-dichloro-5-fluoropyrimidin-2-yl)-2methylimidazo[l,2-a]pyridine (164 mg, 80%) as a yellow solid.
'll NMR (500 MHz, DMSO-rig) δ ppm 9.59 (dt, J = 6.9, 0.9 Hz, 1H), 7.77 (d, J = 8.8 Hz, 1H), 7.62 (t, J = 7.9 Hz, 1H), 7.32 (t, J = 6.9 Hz, 1H), 2.77 (s, 3H); MS m/z 298.1 [M+H]+.
Step 2. 3-(4,6-Dichloro-5-fluoropyrimidin-2-yl)-2-methylimidazo[l,2-a]pyridine (50 mg, 0.168 mmol) and 4-trifluoromethyl aniline (54 mg, 0.336 mmol) were mixed in EtOH (2 mL) and heated in a sealed tube at 100°C until UPLC showed complete consumption of the starting material (48 hours). The reaction mixture was cooled to room temperature and diluted with water (5 mL) to form a precipitate. The product was collected by filtration, then washed with hexanes. The crude product, without drying, was dissolved in CH3CN (2 mL), then saturated ammonia (4 mL) in water was added. The reaction mixture was heated at 100°C in a sealed tube for 16 hours until UPLC showed complete consumption of starting material. A crude product was precipitated by addition of water (10 mL). The precipitate was filtered, then washed with hexanes and dried to yield the title compound (32 mg, 47 % over two steps) as a light tan solid.
]H NMR (500 MHz, Acetone-rig) δ ppm 9.76 (dt, J = 7.1, 1.0 Hz, 1H), 8.50 (br. s., 1H), 7.85 (d, J = 8.5 Hz, 2H), 7.57 (d, J = 8.5 Hz, 2H), 7.40 (d, J = 8.8 Hz, 1H), 7.19 (ddd, J = 8.5, 6.5, 1.8 Hz, 1H), 6.74 (td, J = 6.9, 1.3 Hz, 1H), 6.27 (br. s., 2H), 2.64 (s, 3H); MS m/z 403.3 [M+H]+.
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Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 14 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
170 N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methylimidazo[l,2-a]pyridin-3yl)pyrimidine-4,6-diamine MS m/z 401.3 [M+H]+
171 N-[4-(difhioromethoxy)-3-fluorophenyl]-5-fluoro-2-(2-methylimidazo[l,2-a]pyridin-3yl)pyrimidine-4,6-diamine 'H NMR (500 MHz, DMSO-76) δ ppm 9.83 (d, J = 6.9 Hz, 1H), 9.25 (br. s, 1H), 7.80 (dd, J = 13.4, 2.0 Hz, 1H), 7.57 (d, J = 8.8 Hz, 1H), 7.44 (d, J = 8.5 Hz, 1H), 7.31 - 7.39 (m, 2H), 7.18 (t, J = 73.1 Hz, 1H), 6.88 - 6.97 (m, 3H), 3.31 (s, 3H); MS m/z 419.3 [M+H]+
174 5-fluoro-N-[4-(trifluoromethyl)phenyl]-2-(2,6,8-trimethylimidazo[l,2-a]pyrazin-3yl)pyrimidine-4,6-diamine *H NMR (500 MHz, DMSO-76) δ ppm 9.48 (s, 1H), 9.39 (s, 1H), 7.83 (d, J= 8.51 Hz, 2H), 7.68 (d, J= 8.83 Hz, 2H), 7.11 (s, 2H), 2.75 (s, 3H), 2.72 (s, 3H), 2.55 (s, 3H); m.p. 166-168 °C; MS m/z 432.3 [M+H]+
175 N-[4-(difhioromethoxy)phenyl]-5-fluoro-2-(2,6,8-trimethylimidazo[l,2-a]pyrazin-3yl)pyrimidine-4,6-diamine m.p. 141-143 °C; MS m/z 430.4 [M+H]+
176 N-[4-(difhioromethoxy)-3-fhiorophenyl]-5-fluoro-2-(2,6,8-trimethylimidazo[l,2a]pyrazin-3-yl)pyrimidine-4,6-diamine 'H NMR (500 MHz, DMSO-Jd) δ ppm 9.40 (s, 1H), 9.32 (s, 1H), 7.71 - 7.83 (m, 1H), 7.40 - 7.45 (m, 1H), 7.31 - 7.37 (m, 1H), 7.04- 7.32 (t, J = 70.00 Hz, 1H), 7.07 (s, 2H), 2.74 (s, 3H), 2.72 (s, 3H), 2.38 (s, 3H); m.p. 140-141 °C; MS m/z 448.4 [M+H]+
251 N-(4-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methylimidazo[ 1,2-a]pyridin-3-yl)pyrimidine4,6-diamine ’H NMR (500 MHz, Acetone-dd) δ □ ppm 9.88 - 10.04 (m, 1H), 8.33 - 8.46 (m, 1H), 7.72 (d, J= 8.83 Hz, 2H), 7.48 - 7.59 (m, 1H), 7.39 (d, J= 8.83 Hz, 2H), 7.27 - 7.34 (m, 1H), 6.34 - 6.45 (br., s, 2H), 2.73 (s, 3H); m.p. 226-229 °C; MS m/z 388.2 [M+H]+
252 5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4methoxyphenyl)pyrimidine-4,6-diamine *H NMR (500 MHz, Acetone-z/d) δ ppm 9.91 (dd, J= 2.52, 5.99 Hz, 1H), 8.10 (br. s., 1H), 7.45 - 7.58 ( d, J = 8.83 Hz, 2H ), 7.26 (d, J= 1.89 Hz, 1H), 6.96 (d, J= 8.83 Hz, 2H), 6.23 (br. s., 2H), 3.81 (s, 3H), 2.70 (s, 3H); m.p. 204-206 °C; MS m/z 384.2 [M+H]+
253 5-fluoro-2-(6-fhioro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4-methylphenyl)pyrimidine- 4,6-diamine m.p. 210-212 °C; MS m/z 368.2 [M+H]+
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Example 15
5-chloro-2-(2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine (Cpd 166)
Figure AU2013348009C1_D0191
CF3 cf3
To a solution of 2-(2-methyl-lH-benzo[d]imidazol-l-yl)-N4-(4-(trifluoromethyl)phenyl)pyrimidine-4,6-diamine (76 mg, 0.20 mmol) in DMF (1.5 mL) was added Nchlorosuccinimide (29 mg, 0.22 mmol). The mixture was stirred for 2 hours at room temperature. Ice water (5 mL) and a saturated NaHCO3 solution (2 mL) was added to the mixture. The resulting precipitate was filtered, washed by water, and dried under nitrogen to 10 yield the title compound (77 mg, 92%) as an off-white solid.
‘H NMR (500 MHz, Acetone-76) δ ppm 8.40 (1H, s) 7.95 - 8.00 (1H, m) 7.76 - 7.83 (2H, m) 7.57 (2H, d, 7=8.51 Hz) 7.40 - 7.45 (1H, m) 7.06 - 7.11 (1H, m) 6.98 - 7.04 (1H, m) 6.52 6.75 (2H, m) 2.68 (3H, s); MS m/z 419.1 [M+H]+.
Additional compounds of Formula (I) or a form thereof described herein may be prepared according to the procedure of Example 15 by substituting the appropriate starting materials, reagents and reaction conditions.
Cpd Name & Data
167 5-chloro-2-(2-ethyl-1 H-benzimidazol-1 -yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine 'H NMR (500 MHz, Aceton c-7rt) δ ppm 8.55 (1H, s) 8.07 - 8.12 (1H, m) 7.91 - 7.96 (2H, m) 7.71 (2H, d, 7=8.51 Hz) 7.58 - 7.63 (1H, m) 7.13 - 7.26 (2H, m) 6.80 (2H, br. s.) 3.23 3.30 (2H, m) 1.31 (3H, t, 7=7.41 Hz); MS m/z 433.2 [M+H]+
168 5-chloro-N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-l H-benzimidazol-1-yl)pyrimidine4,6-diamine ]H NMR (500 MHz, Acetone-^) δ ppm 8.31 (1H, s) 8.09 - 8.13 (1H, m) 7.65 - 7.71 (2H, m) 7.55 - 7.60 (1H, m) 7.13 - 7.25 (4H, m) 6.99 (1H, t, 7=74.40 Hz) 6.68 (2H, br. s.) 3.19 - 3.25 (2H, m) 1.28 (3H, t, 7=7.41 Hz); MS m/z 431.2 [M+H]+
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Biological Examples
The following biological examples demonstrate the usefulness of the compounds described herein to inhibit Bmi-1 function and reduce the level of Bmi-1 protein.
Example 1
Sandwich ELISA Assay
Cell Seeding and Compound Treatment (Day 1):
HT-1080 cells were seeded at 8000 cells/well (50 pL) in 96-well tissue culture plates. After the cells became adherent (3-4 hours), 2x diluted stocks of test compounds in 50 pL DMEM containing 1% DMSO (final DMSO concentration was 0.5%) were added and the plates were incubated at 37°C under 5% CO2 for 40-48 hours.
ELISA Plate First Antibody Preparation (Day 2):
The First Antibody (Millipore Mouse, monoclonal to mouse Bmi-1, clone F6, catalog #05-637) diluted to 2 pg/mL in PBS was added (100 pL) to each well of a Nunc MaxiSorp 96-well ELISA plate. The plate was covered with a plate seal and allowed to stand overnight. Cell Lysate Preparation (Day 3):
Fresh lx Lysis buffer was prepared on the day of the assay as follows: 1 mM EDTA, 150 mM NaCl, 0.5% Triton-X 100, 10 mM NaF, 20 mM B-Glycerophosphate, 1 mM DTT (in PBS, pH 7.2-7.4) and lx HALT protease inhibitor cocktail (Pierce #78410).
The lx Lysis Buffer (40 pL) was added to each well and the plate was shaken for 5-10 minutes on an orbital shaker to allow cell lysis, then diluent (1% BSA in PBS in 0.5% NP40) (100 pL) was added to each well.
A standard curve was prepared at the following Bmi-1 concentrations: 8000, 4000, 2000, 1000, 500, 250, 125, 0 pg/mL The Bmi-1 Recombinant Protein Standard (Novus Biologicals PCGF4 Recombinant Protein (P01), catalog # H00000648-P01) used to prepare the standard curve was stored at -80°C. On first thaw, the Bmi-1 Recombinant Protein Standard was diluted to 10 pg/pL in Blocking Buffer (1% BSA in PBS; BSA: Fisher Scientific Catalog #1600-100). Aliquots were taken and refrozen at -80°C. The aliquots may be kept at 4°C and reused after first thaw, but only within 1-2 weeks. The Bmi-1 Recombinant Protein Standard contains a GST-fusion tag that appears around 70 Kda on Western Blot.
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ELISA Assay (Day 3):
The prepared ELISA plate was washed 3x with Wash Buffer (0.05% Tween-20 in PBS). The final wash was removed from the plate and the plate was blotted dry. Blocking Buffer (300 pL) (1% BSA in PBS) was added to each well. The plate was covered with a plate seal and incubated at room temperature for 1 hour. The blocked plate was washed 3x with Wash Buffer, then the final wash was removed and the plate was blotted dry. The previously prepared samples and standards were added (100 μL/well) and the plate was covered with a plate seal and incubated at 4°C overnight.
ELISA Assay (Day 4):
The prepared ELISA plate was removed from 4°C, incubated at room temperature for 30 minutes, then washed and blotted dry as previously described for Day 3. The Second Antibody (Cell Signaling Rabbit anti-Bmi-1, Cat# 2830) diluted to 1:600 in Blocking Buffer was added (100 pL) to each well, except as needed for background control wells. The plate was covered with a plate seal and incubated for 1.5 hrs at room temperature.
The ELISA plate was washed and blotted dry as previously described. The Third Antibody (Cell Signaling HRP conjugated anti-rabbit IgG (Cellsignaling, Cat#:7074) diluted to 1:300 in Blocking Buffer was added (100 pL) to each well, except as needed for background control wells. The plate was incubated for 1 hr at room temperature.
The plate was washed and blotted dry as previously described, then prepared TMB substrate (TMB substrate kit, Pierce catalog #34021) (prepared by mixing kit reagents 1:1) (100 pL) was added per well. The plate was incubated for 20-30 minutes at room temperature in the dark, then Stop Solution (2 M sulfuric acid in water) (50 pL) was added per well. The plates were read at OD450 (experimental) and OD570 (reference).
As shown in Table 1, test compounds described herein had Bmi-1 ELISA EC50 values between > 0.1 pM to < 3 pM (one star), an EC50 value between > 0.01 pM to < 0.1 pM (two stars), an EC50 value between > 0.001 pM to < 0.01 pM (three stars) or an EC50 value of < 0.001 pM (four stars).
Table 1
Cpd EC50 Cpd ECso Cpd ECso Cpd ECso
1 5k 5k 72 5k 5k 143 *** 214 5·: 5k
2 5k 73 5k ik 144 ** 215 J;
3 5k 5k 74 Ji 145 *** 216 5k
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Cpd ECS0 Cpd ECSO Cpd ECso Cpd EC5o
4 ϊ-ί 75 * 146 ^4 217 Ώ4 -T4
5 * 76 ** 147 218 ^54 H4 ^4
6 ** 77 ** 148 * 219 H4
7 * 78 ** 149 J-c ^4 220 ^4 ^4
8 * 79 * 150 ** 221 *
9 *** 80 151 ^4 Ψ 222 ❖
10 81 ** 152 ** 223 *
11 * 82 ** 153 224 **
12 ** 83 ** 154 * 225 **
13 ❖ 84 155 226 *
14 * 85 * 156 44 ^4 227 **
15 ** 86 ** 157 ** 228 **
16 ** 87 * 158 * 229 *
17 * 88 ** 159 * 230 *
18 $ 89 * 160 231 *
19 * 90 * 161 H4 232 **
20 * 91 * 162 ^4 233 ^4 ^4
21 92 ** 163 ^4 234 **
22 ** 93 ** 164 ^4 ^4 235 **
23 * 94 ** 165 *** 236 *
24 * 95 ** 166 * 237 «
25 * 96 * 167 ^4^4 238 *
26 * 97 ** 168 * 239 **
27 * 98 * 169 * 240 ***
28 * 99 * 170 iJ4 241 ^4
29 sji ^4 100 * 171 ^4 242 jJ4
30 * 101 172 * 243
31 ** 102 173 H4 244 <'
32 103 ** 174 ❖ 245 ij4 H4
33 'J4 104 ijc >|c 175 is4 246 H4
34 105 176 * 247 ^4
35 * 106 ^4 177 H4 248 ^4
36 ** 107 178 ❖ 249 H4
37 ^4 108 179 ^4 250 ^4 ^4
38 109 ^4 180 H4 251 ^4
39 110 SJ4 181 ^4 ^4 252 iji
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Cpd ECso Cpd ECso Cpd ECso Cpd ECso
40 111 ^4 182 253 H4 ^4 ^54
41 * 112 ^4 ^4 183 ^4^4 254 5ji ^4
42 ^4 113 44 ^4 184 ^4 ^4 ijc 255 *
43 ** 114 ** 185 256 **
44 * 115 ^4 sjs 186 * 257 **
45 * 116 ** 187 * 258 ^4 ^4 ^4
46 * 117 ** 188 ❖ 259 *
47 * 118 H4 189 * 260 *
48 * 119 Tji 190 * 261 **
49 * 120 ** 191 ** 262 ^4
50 ** 121 ^4 ^4 192 * 263 **
51 ❖ 122 ** 193 ** 264 ***
52 * 123 *** 194 ^4 265 ***
53 * 124 ** 195 * 266 **
54 * 125 * 196 267 *
55 * 126 ** 197 *** 268 *
56 * 127 ** 198 ^4 ^4 ^4 269 *
57 * 128 ^4 ^4 199 270 ***
58 H4 129 ^4 200 *** 271 ***
59 * 130 .** 201 ** 272 **
60 ** 131 ** 202 * 273 ***
61 * 132 ** 203 *** 274 **
62 ** 133 ** 204 ** 275 **
63 ** 134 ** 205 Φ 276 ^4 ^4 ^4
64 ** 135 ** 206 ^4 277 5jc iji
65 ^4 136 207 ^4 ^4 278 •Ϊ*
66 ^4 137 ?|c ?< 208 ^4 i]< iji 279 ^4
67 * 138 ^4 ^4 209 ^4 <4 280 ^4 ^4
68 ^4 H4 139 ^4 210 ^4 281 H4
69 ^4 140 ^4 ^4 211 * 282 if4 sJ4 jJ4
70 * 141 ^4 ^4 212 iJ4 283
71 ** 142 ^4 ^4 213 ^4 ^4 284 Η4 H4
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Example 2
In Vitro Cancer Stem Cell Assay
The effect on inhibition of Bmi-1 function and reduction in the level of Bmi-1 protein by a compound of Formula (I) or a form thereof was tested in the in vitro pediatric Baylor Xenograft Derived (BXD) brain tumor model and in cells from primary patient cultures (PPC).
Cells were grown under conditions to measure either general cell growth (such as in fetal bovine serum (FBS) containing media in conventional tissue culture plates) or in conditions specifically for cancer stem cell (CSC) growth (low serum, nonadherent plates) to assess the effect of Bmi-1 inhibition and reduction in the level of Bmi-1 protein by a compound of Formula (I) on these populations. The cells were treated with a predetermined dose range of Compound 109 at fixed time points over a time period of from 24 hours to 13 days. The effect of inhibition on cell growth viability was quantitated using conventional 2D growth and neurosphere growth using a cell-counting kit (CCK) (supplied by Dojindo Molecular Technologies, Inc.).
Figure 1 demonstrates the effect of Compound 109 in a BXD GBM model where the CSC population (as measured by number of neurospheres) was dose dependently reduced over a period of 13 days in the presence of the stated concentrations of Compound 109.
Figure 2 demonstrates the effect of Compound 109 in a BXD GBM model where the CSC population (as measured by number of neurospheres) was universally reduced over a period of 13 days in the presence of the stated concentrations of Compound 109.
Figure 3 demonstrates the effect of Compound 109 in a tumorosphere assay where 2000 PPC CSCs per well were cultured either under standard 2D tissue culture conditions (with FBS) or conditions selective for CSC growth (attachment-free, serum-free) for 13 days in the presence of the stated concentrations of Compound 109. Both the monolayer and neurosphere CSC populations were reduced as the result of contacting the PPC CSCs with Compound 109, representative of a compound of Formula (I) or a form thereof, at concentrations of 62.5 nm and 15.6 nm, respectively.
Taken together, the data from Figures 1-3 demonstrate the preferential reduction of cancer stem cell populations compared to general cell populations as a result of inhibition of
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Bmi-1 function and reduction in the level of Bmi-1 protein by a compound of Formula (I) or a form thereof.
Example 3
In Vivo Survival Assay
A glioblastoma animal model was developed in which U87-MG tumor cells were injected intracranially into nu/nu mice and a tumor was allowed to become established over a 10 day period. The mice were dosed daily with vehicle, Compound 109 or temozolomide (a standard-of-care agent), as indicated. The comparative results for survival for each treatment group (n = 10) from administration of vehicle, Compound 109 and temozolomide are shown in Figure 4.
Figure 4 demonstrates the effect of daily dosing of Compound 109 compared to temozolomide, at the indicated dose levels, on survival over a 40 day time period in an orthotopic model of glioblastoma. Cells were implanted intracranially into nude mice and dosing was begun 10 days later with either vehicle, Compound 109 or temozolomide. Compound 109 demonstrated extended survival of these tumor bearing mice over both vehicle and temozolomide (p<0.0001).
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WO 2014/081906
PCT/US2013/071132
Without regard to whether a document cited herein was specifically and individually indicated as being incorporated by reference, all documents referred to herein are incorporated by reference into the present application for any and all purposes to the same extent as if each individual reference was fully set forth herein.
Although certain embodiments have been described in detail above, those having ordinary skill in the art will clearly understand that many modifications are possible in the embodiments without departing from the teachings thereof. All such modifications are intended to be encompassed within the scope of the claims presented herein.

Claims (24)

1. A compound of Formula (I):
or a form thereof, wherein
Ri is bicyclic heteroaryl or bicyclic heterocyclyl substituted on a carbon atom ring member with one, two, three or four R5 substituents, or on a nitrogen atom ring member with an oxygen atom substituent to form an N-oxide;
X is N or N substituted with an oxygen atom substituent to form an N-oxide;
R2 is amino;
R3 is hydrogen, cyano, halo, C1 -salkyl, amino, Ci-salkyl-amino or (Ci-8alkyl)2-amino;
R4 is phenyl, optionally substituted with one, two, three or four Re substituents;
Rs is independently selected from the group consisting of cyano, halo, hydroxyl, nitro, oxo,
Ci-salkyl, cyano-Ci-8alkyl, halo-Ci-salkyl, hydroxyl-Ci-salkyl, Ci-8alkoxy, Ci-salkoxy-Ci-salkyl, halo-Ci-salkoxy, C2-salkenyl, Ci-8alkoxy-C2-8alkenyl, C2-salkynyl, Ci-8alkoxy-C2-8alkynyl, carboxyl, amino, Ci-salkyl-amino, (Ci-8alkyl)2-amino, amino-Ci-8alkyl, Ci-salkyl-amino-Ci-salkyl, (Ci-8alkyl)2-amino-Ci-8alkyl, hydroxyl-C 1 -salkyl-amino, hydroxyl-C 1 -salkyl-amino-C 1 -salkyl, hydroxyl-Ci-salkyl-amino-Ci-salkyl-amino, Ci-salkyl-thio, Ci-salkyl-carbonyl, Ci-8alkyl-carbonyl-amino, Ci-salkyl-carbonyl-oxy, Ci-salkyl-carbonyl-oxy-Ci-salkyl, C1 -salkoxy-carbonyl, C1.8alkoxy-carbonyl-C 1 -salkyl, C1 -salkoxy-carbonyl-amino, Ci-salkyl-sulfonyl, C3-i4cycloalkyl, aryl, aryl-Ci-salkyl, aryl-amino, aryl-Ci-salky-amino, heteroaryl, heteroaryl-Ci-salkyl and heterocyclyl, wherein C3-i4cycloalkyl, aryl, heteroaryl or heterocyclyl and the aryl and heteroaryl portions of aryl-Ci-salkyl, aryl-amino, aryl-Ci-salky-amino and heteroaryl-Ci-salkyl are each optionally substituted with one, two, three or four halo, Ci-salkyl, halo-Ci-salkyl, hydroxyl-C 1-salkyl, Ci-salkoxy, halo-Ci-salkoxy, hydroxyl-Cι-salkoxy or carboxyl substituents;
Re is independently selected from the group consisting of cyano, halo, nitro, Ci-salkyl, halo-Ci-salkyl, hydroxyl-C 1-salkyl, Ci-salkoxy, halo-Ci-salkoxy, C2-salkenyl, Ci-8alkoxy-C2-8alkenyl, C2-salkynyl, Ci-salkoxy-C2-salkynyl, carboxyl, formyl, formylAH26( 13743554 1 ):MXC
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2013348009 19 Oct 2017 oxy, Ci.salkyl-carbonyl, halo-C i-salkyl-carbonyl, Ci-salkyl-thio, halo-C i-salkyl-thio, amino, Ci-salkyl-amino, (Ci.salkyfh-amino, Ci^alkyl-carbonyl, C|.salkyl-carbonyl-oxy, C i .salkyl-carbonyl-oxy-C 1 -salkyl, C1 .salkoxy-carbonyl, halo-C 1 .salkoxy-carbonyl, Ci_8alkoxy-carbonyl-Ci_8alkyl, Ci-salkoxy-carbonyl-amino, Ci.salkoxy-carbonyl-amino-Cl.salkyl, amino-carbonyl, Ci-salkyl-amino-carbonyl, (Ci_8alkyl)2-amino-carbonyl, Ci-salkyl-carbonyl-amino, Ci.salkyl-carbonyl-amino-Cl.salkyl, amino-Ci-salkyl, Ci-salkyl-amino-Ci.salkyl, (C i _8alkyl)2-amino-C 1 -salkyl, amino-C 1 .salkyl-amino, C1 .salkyl-amino-C 1 .salkyl-amino, (Ci-salkyl)2-amino-Ci.salkyl-amino, hydroxyl-Ci.salkyl-amino, hydroxyl-Ci.8alkyl-amino-Ci.8alkyl, hydroxyl-Ci.salkyl-amino-Ci.salkyl-amino, imino-C i -salkyl, hydroxyl-imino-C i -salkyl, C i .salkoxy-imino-C i -salkyl, Ci.salkyl-sulfonyl, halo-Ci_salkyl-sulfonyl, amino-sulfonyl, Ci-salkyl-amino-sulfonyl, (Ci_8alkyl)2-amino-sulfonyl, B(ORs)2, C3-i4cycloalkyl, heterocyclyl, aryl and heteroaryl, wherein C3_i4cycloalkyl, heterocyclyl, aryl, and heteroaryl are each optionally substituted with one, two, three or four halo or Ci-salkyl substituents; and
Rs is independently hydrogen or Cj.salkyl;
wherein the form of the compound is selected from the group consisting of a free acid, free base, salt, ester, hydrate, solvate, isotopologue, stereoisomer, racemate, enantiomer, diastereomer and tautomer thereof.
2. The compound or form thereof of claim 1, wherein Ri is substituted bicyclic heteroaryl or bicyclic heterocyclyl selected from the group consisting of lH-indolyl, 2H-indazolyl, 4,5,6,7tetrahydro-2H-indazolyl, lH-benzimidazolyl, imidazo[2,l-b][l,3]thiazolyl, pyrazolo[l,5a]pyridinyl, pyrazolo[l,5-c]pyrimidinyl, imidazof 1,2-a]pyridinyl, 5,6,7,8-tetrahydroimidazo[l,2a]pyridinyl, lH-imidazo[4,5-b]pyridinyl, lH-imidazo[4,5-c]pyridinyl, 4,5,6,7-tetrahydro-3Himidazo[4,5-c]pyridinyl, imidazo[l,2-a]pyrazinyl, imidazo[l,2-a]pyrimidinyl, 7H-purinyl and quinolinyl.
3. The compound or form thereof claim 2, wherein Ri is substituted bicyclic heteroaryl selected from the group consisting of, ΙΗ-indolyl, lH-benzimidazolyl, pyrazolo[l,5-a]pyridinyl, imidazo[l,2-a]pyridinyl, lH-imidazo[4,5-b]pyridinyl, imidazo[l,2-a]pyrazinyl and imidazo[l,2a]pyrimidinyl.
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4. A compound or form thereof, selected from the group consisting of:
2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(5,6-difluoro-2-methyl-l H-benzimidazol- l-yl)-N-[4-(trifhioromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difhioromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidine-4,6diamine
2-[2-(trifhioromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(trifhioromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidine-4,6diamine
2-(6-fhioro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difhioromethoxy)phenyl]-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6diamine
N-[4-(trifhioromethyl)phenyl]-2-(l,3,5-trimethyl-lH-pyrazol-4-yl)pyrimidine-4,6-diamine 2-(6-fhioro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine N-[4-(difhioromethoxy)phenyl]-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(5,6-difhioro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(2-cyclopropyl-6-fluoroimidazo[l,2-a]pyridin-3-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-
4,6-diamine
N-[4-(difhioromethoxy)-3-fluorophenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
2-(2-cyclopropyl-6-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]pyrimidine-4,6-diamine
N-[4-(trifhioromethyl)phenyl]-2-(2,5,6-trimethyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-[3-fhioro-4-(trifhioromethyl)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(2-ethyl-6-fluoro-l H-benzimidazol- l-yl)-N-[4-(trifhioromethyl)phenyl]pyrimidine-4,6-diamine 2-(2-cyclopropyl-6-fluoro-l H-benzimidazol- l-yl)-N-[4-(trifhioromethyl)phenyl]pyrimidine-4,6diamine
2-(2-cyclopropyl-5-fluoro-1 H-benzimidazol-1 -yl)-N-[4-(trifhioromethyl)phenyl]pyrimidine-4,6diamine [3 -(4-amino-6- {[4-(trifluoromethyl)phenyl] amino } pyrimidin-2-yl)-6-fluoroimidazo [ 1,2-a]pyridin-2yl]methanol
2-(6-bromo-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(2,6-dimethyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(6-ethyl-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
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2-(4,6-difluoro-2-methyl-l H-benzimidazol- l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(6-ethenyl-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-fluoro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine-4,6-diamine 2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine-4,6-diamine 2-(6-fluoro-2-methylimidazo[l,2-a]pyrimidin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(difluoromethoxy)phenyl]pyrimidine-4,6-diamine 2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(6-chloro-2-ethyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 5-fluoro-2-(5-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
5-fluoro-2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(5 -fluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
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N- [4-(difluoromethoxy)phenyl] -5 -fluoro-2-(5 -fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-
4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)-3-fluorophenyl]-5fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-
4,6-diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5-fluoropyrimidine-4,6diamine
2-(2-cyclopropyl-1 H-benzimidazol-1 -yl)-N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
2-(5,6-difluoro-2-methyl-1 H-benzimidazol-1 -yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -2-(5,6-difluoro-2-methyl-1 H-benzimidazol-1 -yl)-5 fluoropyrimidine-4,6-diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
2-(2-ethyl-4,6-difluoro-l H-benzimidazol-1-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)-5-fluoropyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
5-fluoro-2-(4-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
4,6-diamine
AH26( 13743554 1 ):MXC
187 □N O O 00
O rj
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(4-fluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2 -methyl- lH-imidazo[4,5-b]pyridin- l-yl)pyrimidine-
4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(2-methyl-1 H-imidazo [4,5 -b]pyridin-1 yl)pyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3-fluorophenyl]-5fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-l H-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-[2-(difluoromethyl)-6-fluoro-lH-benzimidazol-l-yl]pyrimidine-
4,6-diamine
2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(methylsulfanyl)phenyl]pyrimidine-4,6-diamine
2-[2-(l -methylcyclopropyl)-1 H-benzimidazol-1 -yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-[2-(l-methylcyclopropyl)-lH-benzimidazol-l-yl]pyrimidine-4,6diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-[2-(propan-2-yl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-[2-(difluoromethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(2-ethyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5-fluoropyrimidine-
4,6-diamine 2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5-fluoropyrimidine-
4,6-diamine
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2-(2-ethyl-5-fluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-5-fluoro-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
5-chloro-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-chloro-2-(2-ethyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-chloro-N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
5-fluoro-2-(2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(2-methylimidazo [ 1,2-a]pyridin-3 yl)pyrimidine-4,6-diamine
5-methyl-2-(2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methylpyr azolof l,5-a]pyridin-3-yl)pyrimidine-4,6diamine
5-fluoro-N-[4-(trifluoromethyl)phenyl]-2-(2,6,8-trimethylimidazo[l,2-a]pyrazin-3-yl)pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2,6,8-trimethylimidazo[l,2-a]pyrazin-3-yl)pyrimidine-
4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(2,6,8-trimethylimidazo [ 1,2-a]pyrazin-3 yl)pyrimidine-4,6-diamine
5-fluoro-2-(2-methylpyr azolof l,5-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
5 -fluoro-2- [6-fluoro-2-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 -yl] -N- [4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6-diamine
2-(2-cyclopropylpyr azolof l,5-a]pyridin-3-yl)-N-[4-(difluoromethoxy)phenyl]-5-fluoropyrimidine-
4,6-diamine [3 -(4-amino-6- {[4-(difluoromethoxy)phenyl] amino } -5 -fluorop yrimidin-2-yl)-5 -fluorop yrazolo [1,5a]pyridin-2-yl]methanol
2-[2-(methylsulfanyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-l H-benzimidazol-1-yl)-N-[6-(trifluoromethyl)p yridin-3yl]pyrimidine-4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine N-(4-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N- [4-(difluoromethoxy)phenyl] -2-(2-ethyl-5 -fluoropyrazolo [ 1,5 -a]pyridin-3 -y 1)-5-fluorop yrimidine-
4,6-diamine
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2-(2-ethyl-5-fluorop yr azolof l,5-a]pyridin-3-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -2-(2-ethyl-5 -fluorop yrazolo [ 1,5 -a]pyridin-3 -y 1)-5 fluoropyrimidine-4,6-diamine
5-fhioro-2-(6-fhioro-2-methyl-l H-benzimidazol-l-yl)-N-(3-methoxyphenyl)pyrimidine-4,6-diamine N-(3-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
5-fhroro-2-(6-fhroro-2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-
4,6-diamine
4- {[6-amino-5 -fhioro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4- yl] amino (benzonitrile methyl 4- {[6-amino-5 -fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4yl] amino (benzoate
5- fhroro-2-(2-methyl-l H-benzimidazol-l-yl)-N-(3-methylphenyl)pyrimidine-4,6-diamine
5-fhioro-N-(3-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(2-methyl-l H-benzimidazol- l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
N-(4-methoxyphenyl)-2-(2-methyl-l H-benzimidazol- l-yl)pyrimidine-4,6-diamine N-[4-(dimethylamino)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
5-fhroro-2-(2-methyl-l H-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
5-fhioro-N-(4-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-(4-chlorophenyl)-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
4- {[6-amino-5-fluoro-2-(2-methyl-l H-benzimidazol-1 -yl)pyrimidin-4-yl] amino (benzonitrile
5- fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine N-(3-fhioro-4-methoxyphenyl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-(4-chlorophenyl)-2-(2-methyl-l H-benzimidazol- l-yl)pyrimidine-4,6-diamine
4- {[6-amino-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-yl] amino ( benzonitrile
2-(2-methyl-l H-benzimidazol- l-yl)-N-(4-nitrophenyl)pyrimidine-4,6-diamine N-(4-bromophenyl)-2-(2-methyl-l H-benzimidazol- l-yl)pyrimidine-4,6-diamine
2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6diamine
2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
N- [4-(difluoromethoxy)phenyl] -5 -fluoro-2- [2-(methoxymethyl)-1 H-benzimidazol-1 -yl]pyrimidine-
4,6-diamine
5- fhioro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-(4-methylphenyl)pyrimidine-4,6-diamine
5-fhioro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-(4-methoxyphenyl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-5-fluoro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]pyrimidine-4,6-diamine
5-fhioro-2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine
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2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine
1 -(4-amino-5 -fluoro-6- {[4-(trifluoromethyl)phenyl] amino } pyrimidin-2-yl)-2-methyl-1Hbenzimidazole-6-carbonitrile
1 -(4-amino-6- {[4-(difluoromethoxy)phenyl] amino} -5-fluorop yrimidin-2-yl)-2-me thyl- 1Hbenzimidazole-6-carbonitrile l-{4-amino-5-fluoro-6-[(4-methylphenyl)amino]pyrimidin-2-yl} -2 -methyl- lH-benzimidazole-6carbonitrile l-{4-amino-5-fluoro-6-[(4-methoxyphenyl)amino]pyrimidin-2-yl}-2-methyl-lH-benzimidazole-6carbonitrile
1 -(4-amino-6- {[4-(difluoromethoxy)phenyl] amino} -5-fluorop yrimidin-2-yl)-2-me thyl- 1Hbenzimidazole-5-carbonitrile l-{4-amino-5-fluoro-6-[(4-methylphenyl)amino]pyrimidin-2-yl} -2 -methyl- lH-benzimidazole-5carbonitrile l-{4-amino-5-fluoro-6-[(4-methoxyphenyl)amino]pyrimidin-2-yl}-2-methyl-lH-benzimidazole-5carbonitrile
1 -(4-amino-5 -fluoro-6- {[4-(trifluoromethyl)phenyl] amino } pyrimidin-2-yl)-2-methyl-1Hbenzimidazole-5-carbonitrile
1- {4-amino-6-[(4-chlorophenyl)amino]-5-fluoropyrimidin-2-yl} -2 -methyl- lH-benzimidazole-5carbonitrile
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
5-fluoro-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine 5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
5-fluoro-2-(2-methyl-6-nitro-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-(4-chlorophenyl)-2-(4,6-difluoro-2-methyl-l H-benzimidazol-1 -yl)-5-fluoropyrimidine-4,6diamine
2- (4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4- (trifluoromethoxy)phenyl]pyrimidine-4,6-diamine 5-fluoro-N-(4-methoxyphenyl)-2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)pyrimidine-4,6-diamine 2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6diamine
2-(5,7-difluoro-2-methyl-1 H-benzimidazol- l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-(4-chlorophenyl)-5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
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5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
4,6-diamine
5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine 5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6diamine
5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4-methoxyphenyl)pyrimidine-4,6diamine
5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4-methylphenyl)pyrimidine-4,6diamine
5-fluoro-2-(2-methyl-5-nitro-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine 5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-5-nitro-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-diamine 2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5-fluoropyrimidine-
4,6-diamine
2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine N-(4-chlorophenyl)-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine 2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6-diamine N-[4-(dimethylamino)phenyl]-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-(4-chloro-3-fluorophenyl)-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine 2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(3-methylphenyl)pyrimidine-4,6-diamine 2-(2-ethyl-l H-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine 2-(2-ethyl-l H-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-diamine 2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine N-(4-chlorophenyl)-2-(2-ethyl-l H-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine N-(4-chloro-3-fluorophenyl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-diamine 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6diamine
N-(4-chlorophenyl)-2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine
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N-(4-chloro-3-fluorophenyl)-2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
5-fluoro-2-(5-fluoro-2-methyl-l H-benzimidazol- l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine 5-fluoro-2-(5-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6-diamine 5-fhioro-2-(5-fhioro-2-methyl-l H-benzimidazol-l-yl)-N-[4-(trifluoromethoxy)phenyl]pyrimidine-
4,6-diamine, and, 2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine, wherein the form of the compound is selected from the group consisting of a free acid, free base, salt, ester, hydrate, solvate, isotopologue, stereoisomer, racemate, enantiomer, diastereomer and tautomer thereof.
5. A pharmaceutical composition comprising a compound according to any one of claims 1 to 4 or a form thereof in admixture with a pharmaceutically acceptable excipient.
6. A pharmaceutical composition comprising a compound according to claim 4 or a form thereof in admixture with a pharmaceutically acceptable excipient.
7. A method of inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising administering to the subject an effective amount of the compound of any one of claims 1 to 4 or a form thereof.
8. The method of claim 7, further comprising contacting a cell having elevated Bmi-1 levels from the subject with an amount of the compound or form thereof, wherein the cell is selected from the group consisting of a cancer cell, tumor cell, cancer stem cell and tumor stem cell, determining an effective amount of the compound or form thereof that inhibits Bmi-1 function in the cell and subsequently administering the effective amount of the compound or form thereof to the subject.
9. The method of claim 8, wherein the effective amount of the compound or form thereof determined to inhibit Bmi-1 function in the contacted cell reduces Bmi-1 levels in the contacted cell.
10. The method of claim 9, wherein the effective amount of the compound or form thereof is in a range of from about 0.001 mg/Kg/day to about 500 mg/Kg/day.
11. The method of claim 9, wherein the effective amount of the compound or a form thereof is in a range of from about 0.1 ng to about 3500 mg.
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12. The method of any one of claims 7 to 11, comprising administering the compound or form thereof in combination with one or more additional agents selected from the group consisting of anti-cancer agents, anti-proliferative agents, chemotherapeutic agents, immunomodulatory agents, anti-angiogenic agents, anti-inflammatory agents, alkylating agents, steroidal and non-steroidal anti-inflammatory agents, pain relievers, leukotriene antagonists, β2agonists, anticholinergic agents, hormonal agents, biological agents, tubulin binding agents, glucocorticoids, corticosteroid agents, antibacterial agents, antihistamines, anti-malarial agents, anti-viral agents, and antibiotics.
13. A use of the compound of any one of claims 1 to 4 or a form thereof in the manufacture of a medicament for inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising administering an effective amount of the medicament to the subject.
14. A method of inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising administering to the subject an effective amount of the compound of claim 4 or a form thereof.
15. The method of claim 14, further comprising contacting a cell having elevated Bmi-1 levels from the subject with an amount of the compound or form thereof, wherein the cell is selected from the group consisting of a cancer cell, tumor cell, cancer stem cell and tumor stem cell, determining an effective amount of the compound or form thereof that inhibits Bmi-1 function in the cell and subsequently administering the effective amount of the compound or form thereof to the subject.
16. The method of claim 15, wherein the effective amount of the compound or form thereof determined to inhibit Bmi-1 function in the contacted cell reduces Bmi-1 levels in the contacted cell.
17. The method of claim 16, wherein the effective amount of the compound or form thereof is in a range of from about 0.001 mg/Kg/day to about 500 mg/Kg/day.
18. The method of claim 16, wherein the effective amount of the compound or form thereof is in a range of from about 0.1 ng to about 3500 mg.
19. The method of any one of claims 14 to 18, comprising administering the compound or form thereof in combination with one or more additional agents selected from the group consisting of anti-cancer agents, anti-proliferative agents, chemotherapeutic agents,
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20. A use of the compound or form thereof of claim 4 in the manufacture of a medicament for inhibiting Bmi-1 function and reducing the level of Bmi-1 to treat a cancer mediated by Bmi-1 in a subject in need thereof comprising administering an effective amount of the medicament to the subject.
21. The compound of form thereof of claim 1, wherein Ri is bicyclic heteroaryl substituted on a carbon atom ring member with one, two, three or four Rs substituents, or on a nitrogen atom ring member with an oxygen atom substituent to form an N-oxide.
22. The compound or form thereof of claim 1, wherein Ri is bicyclic heterocyclyl substituted on a carbon atom ring member with one, two, three or four Rs substituents, or on a nitrogen atom ring member with an oxygen atom substituent to form an N-oxide, wherein bicyclic heterocyclyl is selected from the group consisting of dihydro-indolyl, indolinyl, tetrahydro-indolyl, dihydroindazolyl, tetrahydro-indazolyl, dihydro-isoindolyl, dihydro-benzofuranyl, tetrahydrobenzofuranyl, dihydro-benzothienyl, tetrahydro-benzothienyl, dihydro-benzoimidazolyl, tetrahydro-benzoimidazolyl, dihydro-benzooxazolyl, tetrahydro-benzooxazolyl, dihydrobenzooxazinyl, tetrahydro-benzooxazinyl, benzofl,3]dioxolyl, benzo[l,4]dioxanyl, benzofl,4]dioxinyl, 4,5,6,7-tetrahydro-2H-indazolyl, 5,6,7,8-tetrahydroimidazo[l,2-a]pyridinyl, 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridinyl, dihydro-purinyl, tetrahydro-purinyl, dihydroquinolinyl, tetrahydro-quinolinyl, dihydro-isoquinolinyl, tetrahydro-isoquinolinyl, dihydroquinazolinyl, tetrahydro-quinazolinyl, dihydro-quinoxalinyl, and tetrahydro-quinoxalinyl.
23. The compound or form thereof of claim 4, selected from the group consisting of 2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(5,6-difhioro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine N-[4-(difluoromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidine-
4,6-diamine 2-[2-(trifhioromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine N-[4-(trifhioromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidine-
4,6-diamine
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2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6diamine
N-[4-(trifluoromethyl)phenyl]-2-(l,3,5-trimethyl-lH-pyrazol-4-yl)pyrimidine-4,6-diamine
2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-(6-fluoro-2-methyl-lH-benzimidazol-1-yl)pyrimidine-4,6diamine
2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(5,6-difluoro-2-methyl-1 H-benzimidazol-1 -yl)-N- [3 -fluoro-4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoroimidazo [ 1,2-a]pyridin-3 -yl)-N- [4-(difluoromethoxy)-3 fluorophenyl]pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -2-(6-fluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -2-(2-ethyl-6-fluoro-1 H-benzimidazol-1 -yl)pyrimidine-
4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3fluorophenyl]pyrimidine-4,6-diamine
N-[4-(trifluoromethyl)phenyl]-2-(2,5,6-trimethyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-[3-fluoro-4-(trifluoromethyl)phenyl]-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
2-(2-ethyl-6-fluoro-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(2-cyclopropyl-6-fluoro-l H-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(2-cyclopropyl-5-fluoro-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine [3 -(4-amino-6- {[4-(trifluoromethyl)phenyl] amino } pyrimidin-2-yl)-6-fluoroimidazo [1,2a]pyridin-2-yl]methanol
2-(6-bromo-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(2,6-dimethyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-ethyl-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-ethenyl-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
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2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(6-fluoro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(6-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine-4,6diamine
2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[3-fluoro-4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(5-chloro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine-4,6diamine
2-(6-fluoro-2-methylimidazo[l,2-a]pyrimidin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4(difluoromethoxy)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
2-(6-chloro-2-ethyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(6-fluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(5 -fluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
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N- [4-(difluoromethoxy)phenyl] -5 -fluoro-2-(5 -fluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
2-(6-chloro-2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)-3-fluorophenyl]5-fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(2-cyclopropyl-1 H-benzimidazol-1 -yl)-N- [4-(difluoromethoxy)phenyl] -5 - fluoropyrimidine -
4,6-diamine
2-(2-cyclopropyl-1 H-benzimidazol-1 -yl)-N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -2-(2-ethyl-1 H-benzimidazol-1 -y 1)-5-fluorop yrimidine-
4,6-diamine
2-(5,6-difluoro-2-methyl-1 H-benzimidazol-1 -yl)-5 -fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -2-(5,6-difluoro-2-methyl-1 H-benzimidazol-1 -y 1)-5 fluoropyrimidine-4,6-diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
2-(2-ethyl-4,6-difluoro-1 H-benzimidazol-1 -yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)-3-fluorophenyl]-2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-4,6-difluoro-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(5,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5fluoropyrimidine-4,6-diamine
5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine4,6-diamine
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N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(4-fluoro-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(4-fluoro-2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
5-fluoro-2-(2-methyl-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(2 -methyl- lH-imidazo[4,5-b]pyridin-1yl)pyrimidine-4,6-diamine
N- [4-(difluoromethoxy)-3 -fluorophenyl] -5 -fluoro-2-(2-methyl-1 H-imidazo [4,5 -b]pyridin-1 yl)pyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-4-fluoro-lH-benzimidazol-l-yl)-N-[4-(difluoromethoxy)-3-fluorophenyl]-5fluoropyrimidine-4,6-diamine
2-(2-cyclopropyl-6-fluoro-l H-benzimidazol- l-yl)-N-[4-(difluoromethoxy)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-(2-ethyl-6-fluoro-lH-benzimidazol-l -yl)pyrimidine-4,6diamine
N-[4-(difluoromethoxy)phenyl]-2-[2-(difluoromethyl)-6-fluoro-lH-benzimidazol-lyl]pyrimidine-4,6-diamine
2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(methylsulfanyl)phenyl]pyrimidine-4,6-diamine
2- [2-( 1 -methylcyclopropyl)-1 H-benzimidazol-1 -yl] -N- [4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-[4-(difluoromethoxy)phenyl]-2-[2-(l-methylcyclopropyl)-lH-benzimidazol-l-yl]pyrimidine-
4,6-diamine
2-(2-cyclopropyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-[2-(methoxymethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-[2-(propan-2-yl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
2-[2-(difluoromethyl)-lH-benzimidazol-l-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6diamine
2-(2-ethyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine 2-(2-cyclopropyl-6-fluoro-lH-imidazo[4,5-b]pyridin-l-yl)-N-[4-(difluoromethoxy)phenyl]-5fluoropyrimidine-4,6-diamine
5 -fluoro-2-(2-methyl-6-nitro-1 H-benzimidazol-1 -yl)-N- [4-(trifluoromethyl)phenyl]pyrimidine-
4,6-diamine
N-(4-chlorophenyl)-2-(4,6-difluoro-2-methyl-l H-benzimidazol-1 -yl)-5-fluoropyrimidine-4,6diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine
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5-fluoro-N-(4-methoxyphenyl)-2-(2-methylpyrazolo[l,5-a]pyridin-3-yl)pyrimidine-4,6-diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6diamine
2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6diamine
2-(5,7-difluoro-2-methyl-l H-benzimidazol-1 -yl)-5-fluoro-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N-(4-chlorophenyl)-5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-[4(trifluoromethoxy)phenyl]pyrimidine-4,6-diamine
N-[4-(difluoromethoxy)phenyl]-5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-lyl)pyrimidine-4,6-diamine
5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6diamine
5-fluoro-2-(6-methoxy-2-methyl-lH-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidine-4,6diamine
5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4-methoxyphenyl)pyrimidine-4,6diamine
5-fluoro-2-(6-fluoro-2-methylimidazo[l,2-a]pyridin-3-yl)-N-(4-methylphenyl)pyrimidine-4,6diamine
5-fluoro-2-(2-methyl-5-nitro-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
5-fluoro-N-(4-methoxyphenyl)-2-(2-methyl-5-nitro-1 H-benzimidazol-1 -yl)pyrimidine-4,6diamine
2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6diamine
2-(6-amino-2-methyl-1 H-benzimidazol-1 -yl)-N-[4-(difluoromethoxy)phenyl] -5 fluoropyrimidine-4,6-diamine
2-(6-amino-2-methyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6diamine
N-(4-chlorophenyl)-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
4,6-diamine
N-(4-chloro-3-fluorophenyl)-5 -fluoro-2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidine-4,6diamine
N-(4-chloro-3-fluorophenyl)-5-fluoro-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
4,6-diamine
N-(4-chlorophenyl)-2-(6-fluoro-2-methyl-l H-benzimidazol- l-yl)pyrimidine-4,6-diamine
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2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6-diamine
2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(4-methoxyphenyl)pyrimidine-4,6-diamine
N-[4-(dimethylamino)phenyl]-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
N-(4-chloro-3-fluorophenyl)-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6diamine
2-(6-fluoro-2-methyl-l H-benzimidazol-l-yl)-N-(3-methylphenyl)pyrimidine-4,6-diamine
2-(2-ethyl-l H-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine
2-(2-ethyl-l H-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-diamine
2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethoxy)phenyl]pyrimidine-4,6diamine
N-(4-chlorophenyl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine N-(4-chloro-3-fluorophenyl)-2-(2-ethyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methylphenyl)pyrimidine-4,6-diamine 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-(4-methoxyphenyl)pyrimidine-4,6-diamine 2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoro-N-[4-(trifluoromethoxy)phenyl]pyrimidine-
4,6-diamine
N-(4-chlorophenyl)-2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6-diamine
N-(4-chloro-3-fluorophenyl)-2-(2-cyclopropyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-4,6diamine, and
5-fluoro-2-(5-fluoro-2-methyl-lH-benzimidazol-l-yl)-N-(4-methylphenyl)pyrimidine-4,6diamine.
24. A compound or form thereof, selected from the group consisting of:
N-(4-methoxyphenyl)-2-(2-methyl-l H-benzimidazol- l-yl)pyrimidin-4-amine
N-(2,3-dihydro-l,4-benzodioxin-6-yl)-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidin-4-amine
2-(2-methylimidazo[l,2-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidin-4-amine
N-(4-methoxyphenyl)-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidin-4-amine
N-(4-chlorophenyl)-2-(2-methylimidazo[l,2-a]pyridin-3-yl)pyrimidin-4-amine
2-(2-methylimidazo[l,2-a]pyridin-3-yl)-N-phenylpyrimidin-4-amine
2-[2-(trifhioromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidin-4amine
N-(4-chlorophenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine
N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine
N-(4-bromophenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine
N-[4-(difhioromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine
N-(4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine
2- [6-chloro-2-(trifhioromethyl)imidazo [ 1,2-a]pyridin-3 -yl] -N- [4(trifluoromethyl)phenyl]pyrimidin-4-amine
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2- [6-chloro-2-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 -yl] -N- [4(trifluoromethoxy)phenyl]pyrimidin-4-amine
N-(4-bromophenyl)-2-[6-chloro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine
2- [6-chloro-2-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 -yl] -N- [4(difluoromethoxy)phenyl]pyrimidin-4-amine
N-(4-chlorophenyl)-2-[6-chloro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine
2-[2-methyl-6-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidin-4-amine
N-(4-bromophenyl)-2-[2-methyl-6-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine
N-(4-methylphenyl)-2-[2-methyl-6-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine
2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-(4-methylphenyl)pyrimidin-4amine
2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-(4-methoxyphenyl)pyrimidin-4amine
2-[5-chloro-l-methyl-2-(trifluoromethyl)-lH-indol-3-yl]-N-(4-methoxyphenyl)pyrimidin-4amine
2-[5-chloro-l-methyl-2-(trifluoromethyl)-lH-indol-3-yl]-N-[4(difluoromethoxy)phenyl]pyrimidin-4-amine
N-(4-bromophenyl)-2-[5-chloro-l-methyl-2-(trifluoromethyl)-lH-indol-3-yl]pyrimidin-4-amine
N-(4-bromophenyl)-2-(6-fluoro-2-phenylimidazo[l,2-a]pyridin-3-yl)pyrimidin-4-amine
2-(6-fluoro-2-phenylimidazo[l,2-a]pyridin-3-yl)-N-(4-methylphenyl)pyrimidin-4-amine
N-(l,3-benzodioxol-5-yl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine
N-(2,3-dihydro-l,4-benzodioxin-6-yl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine
N-(6-methoxypyridin-3-yl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine
N2,N2-dimethyl-N5-{2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-yl}pyridine2,5-diamine
2- [6-bromo-2-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 -yl] -N- [4(trifluoromethyl)phenyl]pyrimidin-4-amine
2-[6-bromo-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-(4-methoxyphenyl)pyrimidin-4amine
N-(3-fluoro-4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine
N-(3-chloro-4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine
N-(3 -chloro-4-methylphenyl)-2- [2-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 -yl]pyrimidin-4amine
N-(4-ethoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine
N-[4-(propan-2-yl)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4-amine
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N- [4-( 1 H-pyrazol-1 -yl)phenyl] -2-[2-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 -yl]pyrimidin-4amine
N-(3-chloro-4-mcthoxyphcnyl)-2-(2-mcthyl-l//-bcnzimidazol-l-yl)pyrimidin-4-aminc
2-(2-methyl-lH-benzimidazol-l-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidin-4-amine
N-(3-chloro-4-methoxyphenyl)-2-[2-(trifluoromethyl)-l H-benzimidazol-l-yl]pyrimidin-4-amine
5-fluoro-N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine
5 -chloro-N-(4-methylphenyl)-2- [2-(trifluoromethyl)imidazo [ 1,2-a]pyridin-3 -yl]pyrimidin-4amine
N-(4-methoxyphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4-amine
2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]-N-[4-(trifluoromethyl)phenyl]pyrimidin-4amine
N-(4-chlorophenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4-amine
2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidin-4-amine
2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethoxy)phenyl]pyrimidin-4-amine
N-(4-methoxyphenyl)-2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]pyrimidin-4amine
N-[4-(difluoromethoxy)phenyl]-2-[6-methoxy-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine
2- {[6- {[4-(difluoromethoxy)phenyl] amino } -2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4yl] amino } ethanol
N-[4-(difluoromethoxy)phenyl]-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4amine
2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3-yl]-N-[4(trifluoromethyl)phenyl]pyrimidin-4-amine
N-[4-(difluoromethoxy)phenyl]-2-[6-fluoro-2-(trifluoromethyl)imidazo[l,2-a]pyridin-3yl]pyrimidin-4-amine
N- [4-(trifluoromethyl)phenyl] -2- [2-(trifluoromethyl)pyrazolo [1,5 -a]pyridin-3 -yl]pyrimidin-4amine
2- {[2-(2-methyl-1 H-benzimidazol-1 -y 1)-6- {[4-(trifluoromethyl)phenyl] amino } pyrimidin-4yl] amino } ethanol
N4-(2-methoxyethyl)-2-(2-methyl-1 H-benzimidazol-1 -yl)-N6-[4(trifluoromethyl)phenyl]pyrimidine-4,6-diamine
N4- [4-(difluoromethoxy)phenyl] -N6-(2-methoxyethyl)-2-(2-methyl-1 H-benzimidazol-1 yl)pyrimidine-4,6-diamine
N-(4-methoxyphenyl)-2-[2-(trifluoromethyl)pyr azolof l,5-a]pyridin-3-yl]pyrimidin-4-amine
N- [4-(difluoromethoxy)phenyl] -2-(2-methyl-1 H-benzimidazol-1 -yl)pyrimidin-4-amine
N-(4-methylphenyl)-2-[2-(trifluoromethyl)imidazo[l,2-a]pyrazin-3-yl]pyrimidin-4-amine
2- {[2-(4,6-difluoro-2-methyl-1 H-benzimidazol-1 -yl)-6- {[4(trifluoromethyl)phenyl] amino } pyrimidin-4-yl] amino } ethanol
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2-(imidazo[l,2-a]pyridin-3-yl)-N-[4-(trifluoromethyl)phenyl]pyrimidin-4-amine
N-(l,3-benzodioxol-5-yl)-5-fluoro-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-(l,3-benzodioxol-5-yl)-2-(2-methyl-l H-benzimidazol-l-yl)pyrimidine-4,6-diamine
N-(2,2-difluoro-l,3-benzodioxol-5-yl)-2-(2 -methyl-1 H-benzimidazol-l-yl)pyrimidine-4,6diamine
N-(6-methoxypyridin-3-yl)-2-(2-methyl-lH-benzimidazol-l-yl)pyrimidine-4,6-diamine N-(l,3-benzodioxol-5-yl)-2-(4,6-difluoro-2-methyl-lH-benzimidazol-l-yl)-5-fluoropyrimidine-
4,6-diamine
N-(l,3-benzodioxol-5-yl)-5-fluoro-2-(6-methoxy-2-methyl-l H-benzimidazol-l-yl)pyrimidine-
4.6- diamine
N-(2,2-difluoro-l,3-benzodioxol-5-yl)-2-(6-fluoro-2-methyl-lH-benzimidazol-l-yl)pyrimidine-
4.6- diamine, and
N-(l, 3-benzodioxol-5-yl)-2-(2-ethyl-l H-benzimidazol- l-yl)-5-fluoropyrimidine-4,6-diamine wherein the form of the compound is selected from the group consisting of salt, ester, hydrate, solvate, chelate, clathrate, polymorph, isotopologue, stereoisomer, racemate, enantiomer, diastereomer and tautomer thereof.
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